Discovery of mammalian genes that participate in virus infection
© Organ et al; licensee BioMed Central Ltd. 2004
Received: 18 June 2004
Accepted: 02 November 2004
Published: 02 November 2004
Viruses are obligate intracellular parasites that rely upon the host cell for different steps in their life cycles. The characterization of cellular genes required for virus infection and/or cell killing will be essential for understanding viral life cycles, and may provide cellular targets for new antiviral therapies.
Candidate genes required for lytic reovirus infection were identified by tagged sequence mutagenesis, a process that permits rapid identification of genes disrupted by gene entrapment. One hundred fifty-one reovirus resistant clones were selected from cell libraries containing 2 × 105 independently disrupted genes, of which 111 contained mutations in previously characterized genes and functionally anonymous transcription units. Collectively, the genes associated with reovirus resistance differed from genes targeted by random gene entrapment in that known mutational hot spots were under represented, and a number of mutations appeared to cluster around specific cellular processes, including: IGF-II expression/signalling, vesicular transport/cytoskeletal trafficking and apoptosis. Notably, several of the genes have been directly implicated in the replication of reovirus and other viruses at different steps in the viral lifecycle.
Tagged sequence mutagenesis provides a rapid, genome-wide strategy to identify candidate cellular genes required for virus infection. The candidate genes provide a starting point for mechanistic studies of cellular processes that participate in the virus lifecycle and may provide targets for novel anti-viral therapies.
Cellular genes are likely to participate in all phases of viral life cycles including attachment to cellular receptors, internalization, disassembly, translation of mRNA, assembly and egress from the cells . The susceptibility to virus infection varies greatly among different cell types, and virus-resistant cells frequently emerge post-infection [2–4]. This suggests that genetic determinants can influence host cell contributions to the virus life cycle. Despite examples of mammalian genes that influence virus infection, the identification of such genes has been hampered by the lack of practical methods for genetic analysis in cultured cells. In the present study, we tested whether tagged sequence mutagenesis – a gene entrapment strategy widely used to mutate genes in mouse embryonic stem cells [5–10] could be used to identify candidate cellular genes required for lytic infection by reovirus, a small cytolytic RNA virus that replicates in the cytoplasm. The mammalian reoviruses serve as useful models for virus-host cell interaction due to their capacity to replicate preferentially in proliferating and undifferentiated cells .
Gene traps are efficient mutagens as assessed by studies in mice of mutations induced originally in embryonic stem cells. In somatic cells, the approach assumes that loss-of-function mutations induced by gene entrapment may confer reovirus resistance as a result of gene dosage effects (e.g. haploinsufficiency), pre-existing heterozygosity or loss of heterozygosity. Following infection with the U3NeoSV1 retrovirus gene trap shuttle vector, libraries of mutagenized rat intestinal epithelial (RIE)-1 cell clones were isolated in which each clone contained a single gene disrupted by provirus integration . The entrapment libraries were infected with reovirus type 1, and virus-resistant clones were selected under conditions that also selected against the emergence of persistently infected cells (PI) that may express virus resistance in the absence of cellular mutations . Genes disrupted in a total of 151 reovirus resistant cells were identified by sequencing regions of genomic DNA adjacent to the entrapment vector ; of these, 111 contained mutations in previously characterized genes and anonymous transcription units.
Reovirus-resistant clones were selected at higher frequencies from entrapment libraries than from non-mutagenized cells, suggesting that reovirus-resistant phenotypes were induced by gene trap mutagenesis. However in any genetic screen, clones with the selected phenotype may arise from spontaneous mutations, and consequently, additional experiments are required to demonstrate that individual genes disrupted by gene entrapment actually contribute to the reovirus-resistant phenotype. For example, a mutation in Ctcf mutation, a transcriptional repressor of insulin growth factor II (IGF-II), was one of 4 mutations associated with reovirus resistance that affected IGF-II expression and/or signalling. Subsequent experiments demonstrated that enforced IGF-II expression is sufficient to confer high levels of reovirus resistance . In short, genes collectively identified by tagged sequence mutagenesis in a panel of reovirus resistant clones provide candidates for mechanistic studies of cellular processes that participate in the virus lifecycle. Since the disrupted genes do not adversely affect cell survival, drugs that inhibit proteins encoded by the genes are not expected to be overtly toxic to cells. Hence, the candidate genes may also include targets for novel anti-viral therapies.
Tagged sequence mutagenesis and selection of reovirus resistant clones
Twenty libraries of mutagenized RIE-1 cells, each representing approximately 104 independent gene trap events, were isolated following infection with the U3NeoSV1 gene trap retrovirus. U3NeoSV1 contains coding sequences for a neomycin resistance gene in the U3 region of the viral long terminal repeat (LTR). Selection for neomycin resistance generates clones with proviruses inserted within actively transcribed genes. Cells pooled from each entrapment library were separately infected with Type 1 reovirus at a multiplicity of infection of 35, and reovirus-resistant clones were selected in serum-free media to suppress the emergence of persistently infected (PI) cells (4). A total of 151 reovirus-resistant clones were isolated – approximately 1 mutant per 103 gene trap clones or 1 mutant per 107 reovirus infected cells. For comparison, the frequency of recovering resistant clones from RIE-1 cells not mutagenized by gene entrapment was less than 10-8. This suggests that reovirus-resistant phenotypes were induced by gene trap mutagenesis.
Identification of genes disrupted in reovirus-resistant clones
The U3NeoSV1 gene trap vector contains a plasmid origin of replication and ampicillin resistance gene; thus, regions of genomic DNA adjacent to the targeting vector were readily cloned by plasmid rescue and sequenced . The flanking sequences were compared to the nucleic acid databases to identify candidate cellular genes that confer resistance to lytic infection by reovirus when altered by gene entrapment. Altogether, the 151 cloned flanking sequences matched 111 annotated gene and transcription units in the public DNA sequence databases [non-redundant (nr), high-throughput genomic sequences (htgs), and human, mouse, and rat genome sequences . 40 flanking sequences were uninformative because they matched repetitive elements or regions of genomic DNA not associated with any annotated transcription unit.
Classification of trapped genes according to function Trapped genes are listed by the official HUGO Gene Nomenclature Committee names, when available. Functional placement of genes or their products are determined by literature assignments. Some genes perform more than one cellular role, and are classified arbitrarily and others have undefined roles.
While the presence of multiple, independent mutations in specific genes provides indirect evidence for their involvement in the reovirus lifecycle, the genes could also represent hot spots for gene entrapment. The U3NeoSV1 vector preferentially targets genes with 5' exons that can splice in-frame with a cryptic splice site in the Neo gene to produce enzymatically active Neo fusion proteins. As a consequence, mutagenesis by U3NeoSV1 is actually quite biased, such that of 400 mutations characterized in ES cells, one-third involved genes disrupted multiple times, including Pecam 1 which was targeted 9 times . However, none of the multiply targeted genes associated with reovirus resistance involved previously observed entrapment hotspots. Conversely, over 10% of the mutations identified in ES cells involved genes for RNA binding proteins, a preference not observed among genes collectively associated with reovirus resistance. Only Madh 7 and Gas5, each represented once among the reovirus-resistant clones, were disrupted by U3NeoSV1 in ES cells. Both genes are commonly targeted by other retroviral gene trap vectors and thus probably represent hot spots for gene entrapment [5, 8].
Potential involvement of disrupted genes in virus replication
The genes associated with reovirus resistance can be grouped according to their presumed role in virus entry, disassembly, translation, and maturation. Reovirus enters the host via an endocytic pathway that requires acidification and proteolysis to remove the viral outer capsid. The presumptive roles of several candidate genes would be anticipated to affect virus replication by interfering with virus disassembly. For example the mannose-6-phosphate receptor/insulin-growth factor-2 receptor (Igf2r) transports cathepsins to the lysosome  and acidification of the lysosome is dependent upon the vacuolar H+-ATPase (Atp6v0c) . NH4Cl is a weak base that interferes with the function of two of the tagged genes, the Igf2r and the Atp6v0c, and blocks the disassembly of reovirus and several other viruses that enter cells via the endocytic pathway. Moreover, specific inhibitors of the vacuolar H+-ATPase gene product have been used to block the infectivity of reovirus and influenza A virus [13, 14]. Four mutations in three different genes [Igf2r, Prss11, a protease associated with insulin binding protein 5, and Ctcf a transcriptional repressor of IGF-II] are predicted to affect IGF-II expression and/or signalling. Cells containing the Ctcf mutation were subsequently found to express elevated levels IGF-II, while enforced IGF-II expression was sufficient to confer high levels of reovirus resistance. The resistance was caused, at least in part, by a block in virus disassembly . Similarly, both anti-IGF-II receptor antibodies and soluble IGF-II receptor have been reported to inhibit herpes simplex virus infection in vitro . By inference, the recovery of several clones with mutations in genes involved in IGF-II expression/signalling pathway suggests that mutations in multiple genes may affect the same phenotype by acting on a common pathway.
Additionally, several of the inserted mutations encode proteins that are thought to participate in trafficking of cargo in cells, and may participate in various stages of virus infection. These include mutations in genes encoding three annexins (Anxa1, Anxa2, Anxa3) and calcyclin (S100a6/S100a1) – proteins that may bind to each other [16–18] – and mutations affecting cytoskeletal and cytoskeletal associated proteins (Cald1, Kif13b, Mapt, Mkln1, Stmn1, Tm9sf4, and Tpm1). Annexin-II associates with cytomegalovirus virions and anti-annexin-II antibodies have been found to prevent cytomegalovirus plaque formation . Annexin-II is known to bind to several of the other gene products mutated in our library. These include annexin-I, calcyclin, and α-tropomysin (Supplementary Table [see Additional File 1]) [17, 18, 20].
One of the clones has a disruption of a novel cell receptor, OL-16, which is a member of the immunoglobulin superfamily [21, 22]. A presumptive cellular receptor for reovirus, junctional adhesion molecule (Jam)-1 , has been shown to bind to all reovirus serotypes , whereas reovirus infection has been found to be host-cell specific . OL-16 is expressed both in L-cells and in RIE-1 cells that can be infected by reovirus type 1 but not in murine erythroleukemia (MEL) cells that are resistant to infection by type 1 reovirus . Forced expression of an OL-16 transgene in MEL cells increases their susceptibility to reovirus type 1 infection (J. Sheng and D. Rubin, unpublished results).
Several of the candidate genes have products that interact with either reovirus or with other viruses (Supplementary Table [see Additional File 1]). Cellular activities involved in post-transcriptional gene regulation may influence the processing or translation of virus transcripts. Two candidate genes participate in these processes. Eif3, part of a multi-subunit translation initiation complex, has been found to specifically bind the 5' end of hepatitis C and classical swine fever virus mRNA . The Cstf 64 KaD subunit, which affects polyadenylation of mRNA, can be cross-linked to the mRNA of herpes simplex mRNA in infected HeLa cell extracts . Other candidate genes are associated with the interferon pathway and host inflammatory responses [28–30]. For example, IκBζ (MAIL), as a component of the NK-κB pathway, may directly or tangentially affect interferon production, inflammation, or apoptosis. In addition, one gene encodes 6-pyruvoyl-tetrahydropterin synthase (Pts), a major regulator of interferon activity  associated with inducible nitric oxide synthase (iNOS). iNOS levels within cells affects the efficiency of replication of many viruses, including the avian reoviruses [32, 33].
Many of the targeted gene products have roles involving the Golgi or endosomal compartments (Figure 3), and additional genes play a role in differentiation or growth arrest. Of these, several are in the transforming growth factor (TGF)-β and NF-κB regulatory pathways, Ppm1a , Madh7 [35–37], Ube1c [38, 39], and Map3k7ip1 [40–43] (Table 1, Supplementary Table [see Additional File 1]). In addition, subunits of the eif3 complex have been functionally linked to Mapkbp1 and the proteosome . We have also disrupted a number of genes that participate in apoptosis (Supplementary Table [see Additional File 1]), and three disrupted genes affect N-linked protein glycosylation, a process that may affect compartmentalization of proteins or ligand interactions.
Reovirus resistant cells have altered susceptibility to HSV-1
Candidate genes required for lytic reovirus infections were identified by tagged sequence mutagenesis, a process that permits rapid identification of genes disrupted by gene entrapment. Since virus-resistant mutants may arise by a variety of mechanisms, additional experiments are needed to demonstrate that individual genes disrupted by gene entrapment actually contribute to the reovirus-resistant phenotype. Even so, several lines of evidence suggest that the genes collectively identified by tagged sequence mutagenesis include cellular activities that participate in the virus lifecycle. First, reovirus-resistant clones were selected at higher frequencies from entrapment libraries than from non-mutagenized cells, suggesting that reovirus-resistant phenotypes were induced by gene trap mutagenesis. Second, the genes associated with reovirus resistance differed from genes targeted in an unselected manner in mouse ES cells. Known mutational hot spots of the U3NeoSV1 were under-represented, and a number of mutations associated with virus resistance appeared to cluster within specific cellular processes and/or affected different components of multi-protein complexes that are likely to play roles in the virus lifecycle. These include IGF-II expression/signalling (3 genes), cytoskeletal/vesicular/trafficking (20 genes), signalling pathways (11 genes), and apoptosis (4 genes). Finally, we recently demonstrated that the disruption of Ctcf, a transcriptional repressor of IGF-II, was directly responsible for reovirus-resistance. In particular, cells containing the Ctcf mutation express elevated levels IGF-II, while parental RIE1 cells forced to express IGF-II acquired high levels of reovirus resistance. The mutation in Ctcf was chosen for further analysis because it was one of 3 mutations affecting IGF-II expression and/or signalling . By inference, the recovery of inserts affecting other genes in the IGF-II signalling pathway suggests that the same phenotype can be achieved through mutations in multiple genes in a common pathway. Taken together, these results suggest that the candidate genes identified by tagged sequence mutagenesis provide useful information to direct mechanistic studies of cellular processes that participate in the virus lifecycle.
These studies utilized a diploid cell line to select for reovirus resistance. Therefore, recessive phenotypes resulting from loss-of-function mutations are generally expected to require separate inactivation of genes carried on both autosomes. In principle this could occur through pre-existing heterozygosity or by loss of the unoccupied allele by one of several mechanisms such as gene conversion, non-disjunction or transcriptional repression. Several of the candidate genes discovered in these experiments are imprinted, and therefore may be anticipated to be mono-allelic in their expression, including the maternally imprinted Igf2r. Alternatively, mutations induced by gene entrapment may confer reovirus resistance as a result of gene dosage effects (e.g. haploinsufficiency). For example, recent data suggests that the most common genetic disease in Caucasians, cystic fibrosis, involves mutations in the ABC-cassette transporter protein, CFTR, that confer resistance to infection by Salmonella typhi . Protection is afforded to persons heterozygous at this allele. Similarly, cyclosporin analogs, which affect P glycoprotein (a member of the ABC cassette transporters), inhibit the growth of Cryptosporidium parum . Of note, one of the genes associated with reovirus resistance identified in the present study, Pgy1 (Abcb1), encodes P glycoprotein (Table 1, Supplementary Table [see Additional File 1]). Finally, while the U3NeoSV1 entrapment vector lacks the MuLV enhancer element, we cannot exclude the possibility that the phenotype observed was related to dominant mutations caused either by transcriptional activation of adjacent cellular genes or from the expression of truncated proteins with dominant-negative activity.
The circumstances that allow gene entrapment to disrupt the function of diploid genes illustrate that events secondary to provirus integration may be required for expression of some reovirus resistant phenotypes. Consequently, while the entrapment libraries were theoretically large enough (2 × 105 independent mutations) to disrupt all expressed genes, it seems unlikely that all the genes that are required for virus infection, and that can be targeted by tagged sequence mutagenesis, were identified in the present study.
Reovirus infection may induce apoptosis in vivo and in vitro, and the suppression of apoptosis enhances the survival of mice infected with reovirus type 3 [49, 50]. Mutations associated with reovirus resistance included a number in proapototic genes including, IκBζ and Bcl2l1; however, the precise role of this pathway and the genes we have disrupted in modulating reovirus infectivity is unknown [51, 52]. Therefore, while many genes are associated with known pathways, further studies will be required to understand the manner by which these pathways influence reovirus infection.
Genetic alterations giving rise to reovirus resistant clones have variable effects on HSV-1 replication, with some reovirus resistant clones showing enhanced HSV1 replication. The reasons for this are unknown, although each of these two viruses enter cells by different mechanisms. The early steps in HSV replication require entry into cells, release of the capsid with migration to the nucleus for which virus and cellular proteins play roles [53, 54], whereas the entry of reovirus does not involve transit to the nucleus. Enhanced HSV-1 replication in clones containing mutations in the S100a6 (calcyclin) and Anxa2 genes was accompanied by a dramatic increase in immediate-early gene expression. This temporal enhancement of HSV-1 replication may reflect activities of calcyclin and annexin 2 proteins that suppress HSV-1 entry [55–57].
In addition to the clone with a mutation in Anxa1, clones with mutations in Eif3s10, Mgat1, and Igf2r also show decreases in transcription and translation of virus mRNA and cell death. Of these, mutations in the Igf2r are known to affect HSV replication [15, 54, 58]; whereas, association of HSV replication with proteins encoded by the Eif3s10, Anxa1, and Mgat1 are novel. These data suggest that some of the candidate genes discovered in clones surviving reovirus infection may affect common cellular processes that are used by other viruses.
Studies in a variety of systems indicate that resistance to infection may be found in nature or achieved in cultured cells. Results presented here support the hypothesis that pathways involved in reovirus infection can be identified through a functional genomics approach based upon insertional mutagenesis. Systematic selection of virus-resistant mutant cells in which the mutant gene can be easily identified may also identify targets for the development of anti-viral therapies. Drugs that disrupt cellular processes may circumvent the problem of virus resistance, generally observed with drugs against virus-encoded proteins. Moreover, since mutations associated with virus resistance are, by necessity, not lethal to the cell, drugs that target the same processes are not expected to have overtly toxic side effects. The fact that the resulting candidate genes may play roles in the replication of other viruses, suggests that different viruses may use similar host proteins for common steps required for virus entry, disassembly, transcription, translation, and reassembly. This view is supported by our studies with HSV-1 and by published reports implicating several of the genes disrupted in reovirus resistant cells (Supplementary Table [see Additional File 1]) in the replication of other viruses. Thus, mutant clones selected for resistance to lytic infection to one virus may provide targets for therapeutics that are active against other families of viruses.
The dramatic increase in the pace of the genome project has led to an explosion of information concerning the sequence of the genome of several species of animals and pathogenic organisms. However, most of the gene sequences have not been functionally ascribed with regard to host-parasite interactions. As there are approximately 30 to 50 × 103 mammalian genes, the definition of function will become the major task facing scientists interested in the relationship between host genes and viral disease over the next decade.
Candidate host genes that participate in lytic virus infections were identified utilizing insertional mutagenesis. Mutant cell clones were recovered that lost their capacity to support virus replication, but were able to proliferate. There was enrichment for genes that were involved in particular metabolic or signalling pathways, with many of the genes being selected more than once from independently derived libraries of RIE-1 cells. Several of the gene products are known to bind to each other. These genes or their products, which are identified by this process of selection, may provide targets for therapeutic intervention.
RIE-1, L-Cells and Virus
Reovirus type 1, strain Lang, was initially obtained from Bernard N. Fields. Virus was passaged in L-cells and a third passaged stock was purified over a CsCl gradient as previously described and was used for these experiments . To develop PI cell lines, RIE-1 cells were infected with reovirus type 1, at a multiplicity of infection (MOI) of 5, and surviving cells were maintained in Dulbecco's modification of Eagle's minimum essential medium (DMEM) (Irvine Scientific, Santa Ana, CA, USA). The herpes simplex virus (HSV)-1 clone, HSV-1 KOStk12, that expresses a reporter gene, lacZ, as an immediate-early gene  was a generous gift of Patricia Spear, Northwestern University, USA. For RIE-1 and L-cells, medium was supplemented with 10% fetal bovine serum, 2 mM per ml, L-Glutamine 100 units per ml, Penicillin, and 100 μg per ml Streptomycin (Irvine Scientific, Santa Ana, CA, USA) [complete medium]. In some experiments, serum was omitted from the medium. The continuance of cell monolayers following infection with reovirus or HSV-1 was determined by staining with gentian violet.
Tagged sequence mutagenesis and selection for reovirus resistance
Following infection of RIE-1 cells with the U3neoSV1 vector, MOI of 0.1, mutagenized cells were selected for neomycin resistance in medium containing 1 mg/ml G418 sulfate (Clontech, Palo Alto, CA, USA) . Twenty libraries of mutant RIE-1 cells, and one library of A549 human adenocarcinoma cells, each consisting of 104 gene entrapment events, were expanded until approximately 103 sibling cells represented each mutant clone. These cells were plated at a sub-confluent density and incubated in serum-free media for 3 days until they became quiescent, and infected with reovirus serotype 1, MOI of 35 plaque forming units (pfu) per cell. Eighteen hours following infection, the cells were detached with trypsin, and plated in DMEM medium containing 10% fetal bovine serum (FBS) (Hyclone Laboratories, Inc., Logan, Utah, USA). After 6 hrs, the medium was removed and cells were maintained in serum-free medium until only a few cells remained attached to the flask. On average, one to ten clones were recovered from a library consisting of 107 mutant cells, an enrichment for selected cells of six orders of magnitude. Cells that survived the selection were transferred to cell culture plates in media containing 10% FBS and cells were divided for extraction of DNA and cryopreservation.
Transcription and translation of HSV-1 immediate early gene reporter
The transcription and translation of the HSV-1 immediate early gene reporter gene, lacZ, was determined by standard northern blot techniques and β-galactosidase assay, respectively.
Generation of libraries of mutagenized RIE-1 cells
Libraries of mutagenized cells were infected with reovirus serotype-1, strain Lang, to select for clones resistant to lytic infection. Selection of virus-resistant clones was performed in serum-free medium to suppress the emergence of persistently infected (PI) cells . This is important since PI cells, which arise by a process involving adaptive mutations in both the virus and the cell genomes , provide a means whereby RIE-1 cells can acquire virus resistance in the absence of cellular mutations. Uninfected RIE-1 cells undergo growth arrest, whereas PI RIE-1 cells are killed in serum-free medium.
DNA sequence analysis
Genomic DNA immediately adjoining the 5' end of the proviral insert in each of 130 cell lines was cloned by plasmid rescue . Approximately 300 to 600 base pairs of this flanking DNA were sequenced and compared with the non-redundant (nr) and expressed sequence tag (dbEST) nucleic acid databases . The probability of a match with orthologous sequences in the databases varies due to interspecies variation, the amount of exon in the flanking DNA (in cases where the flanking DNA matches cDNA sequences), alternative splicing and sequencing errors. Matches with sequences in the database were considered potentially significant if probability score was <10-5 and the sequence was non-repetitive. In most cases, the matching gene was in the same transcriptional orientation as the provirus. Moreover, matches involving cDNA sequences were co-linear across exons present in the flanking genomic DNA and diverged at splice sites. As indicated, virtually all of the genes identified had matches to murine, rat, or human gene sequences with p < 10-10.
This work was supported by Public Health Service Grants (R01NS043952 and R01RR13166 to HER, RO1CA682383 to DHR), by a grant from the Kleberg Foundation, and was partially supported by Cancer Centre (Core) grant P30CA42014, and Avatar BioSci, Inc. We would like to thank P. Spear for the herpes simplex virus used in these experiments. J. Murray and L. Fernandez for advice on the Supplementary Table. J. Hawiger, T. Hodge, and E. Eisenberg for review of the manuscript. B. Mooneyhan provided expert secretarial assistance.
- Op De Beeck A, Caillet-Fauquet P: Viruses and the cell cycle. Prog Cell Cycle Res. 1997, 3: 1-19.View ArticlePubMedGoogle Scholar
- Dermody TS, Nibert ML, Wetzel JD, Tong X, Fields BN: Cells and viruses with mutations affecting viral entry are selected during persistent infections of L cells with mammalian reoviruses. J Virol. 1993, 67: 2055-2063.PubMed CentralPubMedGoogle Scholar
- Taterka J, Sutcliffe M, Rubin DH: Selective reovirus infection of murine hepatocarcinoma cells during cell division. A model of viral liver infection. J Clin Invest. 1994, 94: 353-360.PubMed CentralView ArticlePubMedGoogle Scholar
- Sheng J, Organ EL, Hao C, Wells KS, Ruley HE, Rubin DH: Mutations in the IGF-II pathway that confer resistance to lytic reovirus infection. BMC Cell Biol. 2004, 5: 32-10.1186/1471-2121-5-32.PubMed CentralView ArticlePubMedGoogle Scholar
- Hansen J, Floss T, Van Sloun P, Fuchtbauer EM, Vauti F, Arnold HH, Schnutgen F, Wurst W, von Melchner H, Ruiz P: A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome. Proc Natl Acad Sci U S A. 2003, 100: 9918-9922. 10.1073/pnas.1633296100.PubMed CentralView ArticlePubMedGoogle Scholar
- Hicks GG, Shi EG, Li XM, Li CH, Pawlak M, Ruley HE: Functional genomics in mice by tagged sequence mutagenesis. Nat Genet. 1997, 16: 338-344. 10.1038/ng0897-338.View ArticlePubMedGoogle Scholar
- Salminen M, Meyer BI, Gruss P: Efficient poly A trap approach allows the capture of genes specifically active in differentiated embryonic stem cells and in mouse embryos. Dev Dyn. 1998, 212: 326-333. 10.1002/(SICI)1097-0177(199806)212:2<326::AID-AJA17>3.0.CO;2-1.View ArticlePubMedGoogle Scholar
- Stryke D, Kawamoto M, Huang CC, Johns SJ, King LA, Harper CA, Meng EC, Lee RE, Yee A, L'Italien L, Chuang PT, Young SG, Skarnes WC, Babbitt PC, Ferrin TE: BayGenomics: a resource of insertional mutations in mouse embryonic stem cells. Nucleic Acids Res. 2003, 31: 278-281. 10.1093/nar/gkg064.PubMed CentralView ArticlePubMedGoogle Scholar
- Wiles MV, Vauti F, Otte J, Fuchtbauer EM, Ruiz P, Fuchtbauer A, Arnold HH, Lehrach H, Metz T, von Melchner H, Wurst W: Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells. Nat Genet. 2000, 24: 13-14. 10.1038/71622.View ArticlePubMedGoogle Scholar
- Zambrowicz BP, Friedrich GA, Buxton EC, Lilleberg SL, Person C, Sands AT: Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells. Nature. 1998, 392: 608-611. 10.1038/33423.View ArticlePubMedGoogle Scholar
- Osipovich AB, White-Grindley EK, Hicks GG, Roshon MJ, Shaffer C, Moore JH, Ruley HE: Activation of cryptic 3' splice sites within introns of cellular genes following gene entrapment. Nucleic Acids Res. 2004, 32: 2912-2924. 10.1093/nar/gkh604.PubMed CentralView ArticlePubMedGoogle Scholar
- De Ceuninck F, Poiraudeau S, Pagano M, Tsagris L, Blanchard O, Willeput J, Corvol M: Inhibition of chondrocyte cathepsin B and L activities by insulin-like growth factor-II (IGF-II) and its Ser29 variant in vitro: possible role of the mannose 6-phosphate/IGF-II receptor. Mol Cell Endocrinol. 1995, 113: 205-213. 10.1016/0303-7207(95)03632-H.View ArticlePubMedGoogle Scholar
- Martinez CG, Guinea R, Benavente J, Carrasco L: The entry of reovirus into L cells is dependent on vacuolar proton- ATPase activity. J Virol. 1996, 70: 576-579.PubMed CentralPubMedGoogle Scholar
- Guinea R, Carrasco L: Requirement for vacuolar proton-ATPase activity during entry of influenza virus into cells. J Virol. 1995, 69: 2306-2312.PubMed CentralPubMedGoogle Scholar
- Brunetti CR, Burke RL, Kornfeld S, Gregory W, Masiarz FR, Dingwell KS, Johnson DC: Herpes simplex virus glycoprotein D acquires mannose 6-phosphate residues and binds to mannose 6-phosphate receptors. J Biol Chem. 1994, 269: 17067-17074.PubMedGoogle Scholar
- Zeng FY, Gerke V, Gabius HJ: Identification of annexin II, annexin VI and glyceraldehyde-3-phosphate dehydrogenase as calcyclin-binding proteins in bovine heart. Int J Biochem. 1993, 25: 1019-1027. 10.1016/0020-711X(93)90116-V.View ArticlePubMedGoogle Scholar
- Lee KH, Na DS, Kim JW: Calcium-dependent interaction of annexin I with annexin II and mapping of the interaction sites. FEBS Lett. 1999, 442: 143-146. 10.1016/S0014-5793(98)01643-3.View ArticlePubMedGoogle Scholar
- Filipek A, Wojda U, Lesniak W: Interaction of calcyclin and its cyanogen bromide fragments with annexin II and glyceraldehyde 3-phosphate dehydrogenase. Int J Biochem Cell Biol. 1995, 27: 1123-1131. 10.1016/1357-2725(95)00096-8.View ArticlePubMedGoogle Scholar
- Pietropaolo RL, Compton T: Direct interaction between human cytomegalovirus glycoprotein B and cellular annexin II. J Virol. 1997, 71: 9803-9807.PubMed CentralPubMedGoogle Scholar
- Golitsina NL, Kordowska J, Wang CL, Lehrer SS: Ca2+-dependent binding of calcyclin to muscle tropomyosin. Biochem Biophys Res Commun. 1996, 220: 360-365. 10.1006/bbrc.1996.0410.View ArticlePubMedGoogle Scholar
- Hida K, Wada J, Zhang H, Hiragushi K, Tsuchiyama Y, Shikata K, Makino H: Identification of genes specifically expressed in the accumulated visceral adipose tissue of OLETF rats. J Lipid Res. 2000, 41: 1615-1622.PubMedGoogle Scholar
- Katoh M: IGSF11 gene, frequently up-regulated in intestinal-type gastric cancer, encodes adhesion molecule homologous to CXADR, FLJ22415 and ESAM. Int J Oncol. 2003, 23: 525-531.PubMedGoogle Scholar
- Barton ES, Forrest JC, Connolly JL, Chappell JD, Liu Y, Schnell FJ, Nusrat A, Parkos CA, Dermody TS: Junction adhesion molecule is a receptor for reovirus. Cell. 2001, 104: 441-451. 10.1016/S0092-8674(01)00231-8.View ArticlePubMedGoogle Scholar
- Weiner HL, Powers ML, Fields BN: Absolute linkage of virulence and central nervous system cell tropism of reoviruses to viral hemagglutinin. J Infect Dis. 1980, 141: 609-616.View ArticlePubMedGoogle Scholar
- Rubin DH, Wetzel JD, Williams WV, Cohen JA, Dworkin C, Dermody TS: Binding of type 3 reovirus by a domain of the sigma 1 protein important for hemagglutination leads to infection of murine erythroleukemia cells. J Clin Invest. 1992, 90: 2536-2542.PubMed CentralView ArticlePubMedGoogle Scholar
- Sizova DV, Kolupaeva VG, Pestova TV, Shatsky IN, Hellen CU: Specific interaction of eukaryotic translation initiation factor 3 with the 5' nontranslated regions of hepatitis C virus and classical swine fever virus RNAs. J Virol. 1998, 72: 4775-4782.PubMed CentralPubMedGoogle Scholar
- McGregor F, Phelan A, Dunlop J, Clements JB: Regulation of herpes simplex virus poly (A) site usage and the action of immediate-early protein IE63 in the early-late switch. J Virol. 1996, 70: 1931-1940.PubMed CentralPubMedGoogle Scholar
- Pitha PM, Au WC, Lowther W, Juang YT, Schafer SL, Burysek L, Hiscott J, Moore PA: Role of the interferon regulatory factors (IRFs) in virus-mediated signaling and regulation of cell growth. Biochimie. 1998, 80: 651-658. 10.1016/S0300-9084(99)80018-2.View ArticlePubMedGoogle Scholar
- Hawiger J: Innate immunity and inflammation: a transcriptional paradigm. Immunol Res. 2001, 23: 99-109. 10.1385/IR:23:2-3:099.View ArticlePubMedGoogle Scholar
- Lau JF, Horvath CM: Mechanisms of Type I interferon cell signaling and STAT-mediated transcriptional responses. Mt Sinai J Med. 2002, 69: 156-168.PubMedGoogle Scholar
- Werner-Felmayer G, Werner ER, Fuchs D, Hausen A, Reibnegger G, Schmidt K, Weiss G, Wachter H: Pteridine biosynthesis in human endothelial cells. Impact on nitric oxide-mediated formation of cyclic GMP. J Biol Chem. 1993, 268: 1842-1846.PubMedGoogle Scholar
- Reiss CS, Komatsu T: Does nitric oxide play a critical role in viral infections?. J Virol. 1998, 72: 4547-4551.PubMed CentralPubMedGoogle Scholar
- Pertile TL, Karaca K, Sharma JM, Walser MM: An antiviral effect of nitric oxide: inhibition of reovirus replication. Avian Dis. 1996, 40: 342-348.View ArticlePubMedGoogle Scholar
- Takekawa M, Maeda T, Saito H: Protein phosphatase 2Calpha inhibits the human stress-responsive p38 and JNK MAPK pathways. Embo J. 1998, 17: 4744-4752. 10.1093/emboj/17.16.4744.PubMed CentralView ArticlePubMedGoogle Scholar
- Rousse S, Lallemand F, Montarras D, Pinset C, Mazars A, Prunier C, Atfi A, Dubois C: Transforming growth factor-beta inhibition of insulin-like growth factor-binding protein-5 synthesis in skeletal muscle cells involves a c-Jun N-terminal kinase-dependent pathway. J Biol Chem. 2001, 276: 46961-46967. 10.1074/jbc.M104440200.View ArticlePubMedGoogle Scholar
- Uchida K, Suzuki H, Ohashi T, Nitta K, Yumura W, Nihei H: Involvement of MAP kinase cascades in Smad7 transcriptional regulation. Biochem Biophys Res Commun. 2001, 289: 376-381. 10.1006/bbrc.2001.5984.View ArticlePubMedGoogle Scholar
- Arsura M, Panta GR, Bilyeu JD, Cavin LG, Sovak MA, Oliver AA, Factor V, Heuchel R, Mercurio F, Thorgeirsson SS, Sonenshein GE: Transient activation of NF-kappaB through a TAK1/IKK kinase pathway by TGF-beta1 inhibits AP-1/SMAD signaling and apoptosis: implications in liver tumor formation. Oncogene. 2003, 22: 412-425. 10.1038/sj.onc.1206132.View ArticlePubMedGoogle Scholar
- Amir RE, Iwai K, Ciechanover A: The NEDD8 pathway is essential for SCF(beta -TrCP)-mediated ubiquitination and processing of the NF-kappa B precursor p105. J Biol Chem. 2002, 277: 23253-23259. 10.1074/jbc.M200967200.View ArticlePubMedGoogle Scholar
- Tanaka K, Kawakami T, Tateishi K, Yashiroda H, Chiba T: Control of IkappaBalpha proteolysis by the ubiquitin-proteasome pathway. Biochimie. 2001, 83: 351-356. 10.1016/S0300-9084(01)01237-8.View ArticlePubMedGoogle Scholar
- Sakurai H, Shigemori N, Hasegawa K, Sugita T: TGF-beta-activated kinase 1 stimulates NF-kappa B activation by an NF-kappa B-inducing kinase-independent mechanism. Biochem Biophys Res Commun. 1998, 243: 545-549. 10.1006/bbrc.1998.8124.View ArticlePubMedGoogle Scholar
- Shibuya H, Yamaguchi K, Shirakabe K, Tonegawa A, Gotoh Y, Ueno N, Irie K, Nishida E, Matsumoto K: TAB1: an activator of the TAK1 MAPKKK in TGF-beta signal transduction. Science. 1996, 272: 1179-1182.View ArticlePubMedGoogle Scholar
- Bhat NR, Shen Q, Fan F: TAK1-mediated induction of nitric oxide synthase gene expression in glial cells. J Neurochem. 2003, 87: 238-247. 10.1046/j.1471-4159.2003.01998.x.View ArticlePubMedGoogle Scholar
- Yanagisawa M, Nakashima K, Takeda K, Ochiai W, Takizawa T, Ueno M, Takizawa M, Shibuya H, Taga T: Inhibition of BMP2-induced, TAK1 kinase-mediated neurite outgrowth by Smad6 and Smad7. Genes Cells. 2001, 6: 1091-1099. 10.1046/j.1365-2443.2001.00483.x.View ArticlePubMedGoogle Scholar
- Asano K, Vornlocher HP, Richter-Cook NJ, Merrick WC, Hinnebusch AG, Hershey JW: Structure of cDNAs encoding human eukaryotic initiation factor 3 subunits. Possible roles in RNA binding and macromolecular assembly. J Biol Chem. 1997, 272: 27042-27052. 10.1074/jbc.272.43.27042.View ArticlePubMedGoogle Scholar
- Higaki S, Gebhardt BM, Lukiw WJ, Thompson HW, Hill JM: Effect of immunosuppression on gene expression in the HSV-1 latently infected mouse trigeminal ganglion. Invest Ophthalmol Vis Sci. 2002, 43: 1862-1869.PubMedGoogle Scholar
- Spear BT, Longley T, Moulder S, Wang SL, Peterson ML: A sensitive lacZ-based expression vector for analyzing transcriptional control elements in eukaryotic cells. DNA Cell Biol. 1995, 14: 635-642.View ArticlePubMedGoogle Scholar
- Pier GB, Grout M, Zaidi T, Meluleni G, Mueschenborn SS, Banting G, Ratcliff R, Evans MJ, Colledge WH: Salmonella typhi uses CFTR to enter intestinal epithelial cells. Nature. 1998, 393: 79-82. 10.1038/30006.View ArticlePubMedGoogle Scholar
- Perkins ME, Wu TW, Le Blancq SM: Cyclosporin analogs inhibit in vitro growth of Cryptosporidium parvum. Antimicrob Agents Chemother. 1998, 42: 843-848.PubMed CentralPubMedGoogle Scholar
- Clarke P, Tyler KL: Reovirus-induced apoptosis: A minireview. Apoptosis. 2003, 8: 141-150. 10.1023/A:1022966508671.View ArticlePubMedGoogle Scholar
- Richardson-Burns SM, Tyler KL: Regional differences in viral growth and central nervous system injury correlate with apoptosis. J Virol. 2004, 78: 5466-5475. 10.1128/JVI.78.10.5466-5475.2004.PubMed CentralView ArticlePubMedGoogle Scholar
- Clarke P, Meintzer SM, Widmann C, Johnson GL, Tyler KL: Reovirus infection activates JNK and the JNK-dependent transcription factor c-Jun. J Virol. 2001, 75: 11275-11283. 10.1128/JVI.75.23.11275-11283.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Clarke P, Meintzer SM, Moffitt LA, Tyler KL: Two distinct phases of virus-induced nuclear factor kappa B regulation enhance tumor necrosis factor-related apoptosis-inducing ligand-mediated apoptosis in virus-infected cells. J Biol Chem. 2003, 278: 18092-18100. 10.1074/jbc.M300265200.View ArticlePubMedGoogle Scholar
- Bender FC, Whitbeck JC, Ponce de Leon M, Lou H, Eisenberg RJ, Cohen GH: Specific association of glycoprotein B with lipid rafts during herpes simplex virus entry. J Virol. 2003, 77: 9542-9552. 10.1128/JVI.77.17.9542-9552.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhou G, Avitabile E, Campadelli-Fiume G, Roizman B: The domains of glycoprotein D required to block apoptosis induced by herpes simplex virus 1 are largely distinct from those involved in cell-cell fusion and binding to nectin1. J Virol. 2003, 77: 3759-3767. 10.1128/JVI.77.6.3759-3767.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Schelling JR, Gentry DJ, Dubyak GR: Annexin II inhibition of G protein-regulated inositol trisphosphate formation in rat aortic smooth muscle. Am J Physiol. 1996, 270: F682-90.PubMedGoogle Scholar
- Babiychuk EB, Monastyrskaya K, Burkhard FC, Wray S, Draeger A: Modulating signaling events in smooth muscle: cleavage of annexin 2 abolishes its binding to lipid rafts. Faseb J. 2002, 16: 1177-1184. 10.1096/fj.02-0070com.View ArticlePubMedGoogle Scholar
- Pittis MG, Muzzolin L, Giulianini PG, Garcia RC: Mycobacteria-containing phagosomes associate less annexins I, VI, VII and XI, but not II, concomitantly with a diminished phagolysosomal fusion. Eur J Cell Biol. 2003, 82: 9-17.View ArticlePubMedGoogle Scholar
- Brunetti CR, Dingwell KS, Wale C, Graham FL, Johnson DC: Herpes simplex virus gD and virions accumulate in endosomes by mannose 6-phosphate-dependent and -independent mechanisms. J Virol. 1998, 72: 3330-3339.PubMed CentralPubMedGoogle Scholar
- Rubin DH, Kornstein MJ, Anderson AO: Reovirus serotype 1 intestinal infection: a novel replicative cycle with ileal disease. J Virol. 1985, 53: 391-398.PubMed CentralPubMedGoogle Scholar
- Ahmed R, Canning WM, Kauffman RS, Sharpe AH, Hallum JV, Fields BN: Role of the host cell in persistent viral infection: coevolution of L cells and reovoirus during persistent infection. Cell. 1981, 25: 325-332. 10.1016/0092-8674(81)90050-7.View ArticlePubMedGoogle Scholar
- Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997, 25: 3389-3402. 10.1093/nar/25.17.3389.PubMed CentralView ArticlePubMedGoogle Scholar
- Emans N, Gorvel JP, Walter C, Gerke V, Kellner R, Griffiths G, Gruenberg J: Annexin II is a major component of fusogenic endosomal vesicles. J Cell Biol. 1993, 120: 1357-1369. 10.1083/jcb.120.6.1357.View ArticlePubMedGoogle Scholar
- Fiedler K, Kellner R, Simons K: Mapping the protein composition of trans-Golgi network (TGN)-derived carrier vesicles from polarized MDCK cells. Electrophoresis. 1997, 18: 2613-2619.View ArticlePubMedGoogle Scholar
- Nezu J, Motojima K, Tamura H, Ohkuma S: Molecular cloning of a rat liver cDNA encoding the 16 kDa subunit of vacuolar H(+)-ATPases: organellar and tissue distribution of 16 kDa proteolipids. J Biochem (Tokyo). 1992, 112: 212-219.Google Scholar
- Orci L, Perrelet A, Rothman JE: Vesicles on strings: morphological evidence for processive transport within the Golgi stack. Proc Natl Acad Sci U S A. 1998, 95: 2279-2283. 10.1073/pnas.95.5.2279.PubMed CentralView ArticlePubMedGoogle Scholar
- Nakamura N, Lowe M, Levine TP, Rabouille C, Warren G: The vesicle docking protein p115 binds GM130, a cis-Golgi matrix protein, in a mitotically regulated manner. Cell. 1997, 89: 445-455. 10.1016/S0092-8674(00)80225-1.View ArticlePubMedGoogle Scholar
- Okutsu T, Kuroiwa Y, Kagitani F, Kai M, Aisaka K, Tsutsumi O, Kaneko Y, Yokomori K, Surani MA, Kohda T, Kaneko-Ishino T, Ishino F: Expression and imprinting status of human PEG8/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms' tumors. J Biochem (Tokyo). 2000, 127: 475-483.View ArticleGoogle Scholar
- Kumar R, Yang J, Larsen RD, Stanley P: Cloning and expression of N-acetylglucosaminyltransferase I, the medial Golgi transferase that initiates complex N-linked carbohydrate formation. Proc Natl Acad Sci U S A. 1990, 87: 9948-9952.PubMed CentralView ArticlePubMedGoogle Scholar
- Nilsson T, Rabouille C, Hui N, Watson R, Warren G: The role of the membrane-spanning domain and stalk region of N- acetylglucosaminyltransferase I in retention, kin recognition and structural maintenance of the Golgi apparatus in HeLa cells. J Cell Sci. 1996, 109: 1975-1989.PubMedGoogle Scholar
- Nilsson T, Slusarewicz P, Hoe MH, Warren G: Kin recognition. A model for the retention of Golgi enzymes. FEBS Lett. 1993, 330: 1-4. 10.1016/0014-5793(93)80906-B.View ArticlePubMedGoogle Scholar
- Yang W, Pepperkok R, Bender P, Kreis TE, Storrie B: Modification of the cytoplasmic domain affects the subcellular localization of Golgi glycosyl-transferases. Eur J Cell Biol. 1996, 71: 53-61.PubMedGoogle Scholar
- Hirst J, Futter CE, Hopkins CR: The kinetics of mannose 6-phosphate receptor trafficking in the endocytic pathway in HEp-2 cells: the receptor enters and rapidly leaves multivesicular endosomes without accumulating in a prelysosomal compartment. Mol Biol Cell. 1998, 9: 809-816.PubMed CentralView ArticlePubMedGoogle Scholar
- Sheng Q, Denis D, Ratnofsky M, Roberts TM, DeCaprio JA, Schaffhausen B: The DnaJ domain of polyomavirus large T antigen is required to regulate Rb family tumor suppressor function. J Virol. 1997, 71: 9410-9416.PubMed CentralPubMedGoogle Scholar
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