Skip to main content
Genetics logoLink to Genetics
. 2001 May;158(1):123–132. doi: 10.1093/genetics/158.1.123

Minimum requirements for the function of eukaryotic translation initiation factor 2.

F L Erickson 1, J Nika 1, S Rippel 1, E M Hannig 1
PMCID: PMC1461651  PMID: 11333223

Abstract

Eukaryotic translation initiation factor 2 (eIF2) is a G protein heterotrimer required for GTP-dependent delivery of initiator tRNA to the ribosome. eIF2B, the nucleotide exchange factor for eIF2, is a heteropentamer that, in yeast, is encoded by four essential genes and one nonessential gene. We found that increased levels of wild-type eIF2, in the presence of sufficient levels of initiator tRNA, overcome the requirement for eIF2B in vivo. Consistent with bypassing eIF2B, these conditions also suppress the lethal effect of overexpressing the mammalian tumor suppressor PKR, an eIF2alpha kinase. The effects described are further enhanced in the presence of a mutation in the G protein (gamma) subunit of eIF2, gcd11-K250R, which mimics the function of eIF2B in vitro. Interestingly, the same conditions that bypass eIF2B also overcome the requirement for the normally essential eIF2alpha structural gene (SUI2). Our results suggest that the eIF2betagamma complex is capable of carrying out the essential function(s) of eIF2 in the absence of eIF2alpha and eIF2B and are consistent with the idea that the latter function primarily to regulate the level of eIF2.GTP.Met-tRNA(i)(Met) ternary complexes in vivo.

Full Text

The Full Text of this article is available as a PDF (408.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barber G. N., Jagus R., Meurs E. F., Hovanessian A. G., Katze M. G. Molecular mechanisms responsible for malignant transformation by regulatory and catalytic domain variants of the interferon-induced enzyme RNA-dependent protein kinase. J Biol Chem. 1995 Jul 21;270(29):17423–17428. doi: 10.1074/jbc.270.29.17423. [DOI] [PubMed] [Google Scholar]
  2. Boeke J. D., Trueheart J., Natsoulis G., Fink G. R. 5-Fluoroorotic acid as a selective agent in yeast molecular genetics. Methods Enzymol. 1987;154:164–175. doi: 10.1016/0076-6879(87)54076-9. [DOI] [PubMed] [Google Scholar]
  3. Bourne H. R., Sanders D. A., McCormick F. The GTPase superfamily: conserved structure and molecular mechanism. Nature. 1991 Jan 10;349(6305):117–127. doi: 10.1038/349117a0. [DOI] [PubMed] [Google Scholar]
  4. Brostrom C. O., Prostko C. R., Kaufman R. J., Brostrom M. A. Inhibition of translational initiation by activators of the glucose-regulated stress protein and heat shock protein stress response systems. Role of the interferon-inducible double-stranded RNA-activated eukaryotic initiation factor 2alpha kinase. J Biol Chem. 1996 Oct 4;271(40):24995–25002. doi: 10.1074/jbc.271.40.24995. [DOI] [PubMed] [Google Scholar]
  5. Bushman J. L., Asuru A. I., Matts R. L., Hinnebusch A. G. Evidence that GCD6 and GCD7, translational regulators of GCN4, are subunits of the guanine nucleotide exchange factor for eIF-2 in Saccharomyces cerevisiae. Mol Cell Biol. 1993 Mar;13(3):1920–1932. doi: 10.1128/mcb.13.3.1920. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bushman J. L., Foiani M., Cigan A. M., Paddon C. J., Hinnebusch A. G. Guanine nucleotide exchange factor for eukaryotic translation initiation factor 2 in Saccharomyces cerevisiae: interactions between the essential subunits GCD2, GCD6, and GCD7 and the regulatory subunit GCN3. Mol Cell Biol. 1993 Aug;13(8):4618–4631. doi: 10.1128/mcb.13.8.4618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chakrabarti A., Maitra U. Release and recycling of eukaryotic initiation factor 2 in the formation of an 80 S ribosomal polypeptide chain initiation complex. J Biol Chem. 1992 Jun 25;267(18):12964–12972. [PubMed] [Google Scholar]
  8. Chong K. L., Feng L., Schappert K., Meurs E., Donahue T. F., Friesen J. D., Hovanessian A. G., Williams B. R. Human p68 kinase exhibits growth suppression in yeast and homology to the translational regulator GCN2. EMBO J. 1992 Apr;11(4):1553–1562. doi: 10.1002/j.1460-2075.1992.tb05200.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cigan A. M., Bushman J. L., Boal T. R., Hinnebusch A. G. A protein complex of translational regulators of GCN4 mRNA is the guanine nucleotide-exchange factor for translation initiation factor 2 in yeast. Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5350–5354. doi: 10.1073/pnas.90.11.5350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Cigan A. M., Foiani M., Hannig E. M., Hinnebusch A. G. Complex formation by positive and negative translational regulators of GCN4. Mol Cell Biol. 1991 Jun;11(6):3217–3228. doi: 10.1128/mcb.11.6.3217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Cigan A. M., Pabich E. K., Feng L., Donahue T. F. Yeast translation initiation suppressor sui2 encodes the alpha subunit of eukaryotic initiation factor 2 and shares sequence identity with the human alpha subunit. Proc Natl Acad Sci U S A. 1989 Apr;86(8):2784–2788. doi: 10.1073/pnas.86.8.2784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dever T. E., Chen J. J., Barber G. N., Cigan A. M., Feng L., Donahue T. F., London I. M., Katze M. G., Hinnebusch A. G. Mammalian eukaryotic initiation factor 2 alpha kinases functionally substitute for GCN2 protein kinase in the GCN4 translational control mechanism of yeast. Proc Natl Acad Sci U S A. 1993 May 15;90(10):4616–4620. doi: 10.1073/pnas.90.10.4616. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dever T. E., Feng L., Wek R. C., Cigan A. M., Donahue T. F., Hinnebusch A. G. Phosphorylation of initiation factor 2 alpha by protein kinase GCN2 mediates gene-specific translational control of GCN4 in yeast. Cell. 1992 Feb 7;68(3):585–596. doi: 10.1016/0092-8674(92)90193-g. [DOI] [PubMed] [Google Scholar]
  14. Dever T. E., Glynias M. J., Merrick W. C. GTP-binding domain: three consensus sequence elements with distinct spacing. Proc Natl Acad Sci U S A. 1987 Apr;84(7):1814–1818. doi: 10.1073/pnas.84.7.1814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Dever T. E., Yang W., Aström S., Byström A. S., Hinnebusch A. G. Modulation of tRNA(iMet), eIF-2, and eIF-2B expression shows that GCN4 translation is inversely coupled to the level of eIF-2.GTP.Met-tRNA(iMet) ternary complexes. Mol Cell Biol. 1995 Nov;15(11):6351–6363. doi: 10.1128/mcb.15.11.6351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Donahue T. F., Cigan A. M., Pabich E. K., Valavicius B. C. Mutations at a Zn(II) finger motif in the yeast eIF-2 beta gene alter ribosomal start-site selection during the scanning process. Cell. 1988 Aug 26;54(5):621–632. doi: 10.1016/s0092-8674(88)80006-0. [DOI] [PubMed] [Google Scholar]
  17. Donzé O., Jagus R., Koromilas A. E., Hershey J. W., Sonenberg N. Abrogation of translation initiation factor eIF-2 phosphorylation causes malignant transformation of NIH 3T3 cells. EMBO J. 1995 Aug 1;14(15):3828–3834. doi: 10.1002/j.1460-2075.1995.tb00052.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Dorris D. R., Erickson F. L., Hannig E. M. Mutations in GCD11, the structural gene for eIF-2 gamma in yeast, alter translational regulation of GCN4 and the selection of the start site for protein synthesis. EMBO J. 1995 May 15;14(10):2239–2249. doi: 10.1002/j.1460-2075.1995.tb07218.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Engelberg D., Klein C., Martinetto H., Struhl K., Karin M. The UV response involving the Ras signaling pathway and AP-1 transcription factors is conserved between yeast and mammals. Cell. 1994 May 6;77(3):381–390. doi: 10.1016/0092-8674(94)90153-8. [DOI] [PubMed] [Google Scholar]
  20. Erickson F. L., Hannig E. M. Ligand interactions with eukaryotic translation initiation factor 2: role of the gamma-subunit. EMBO J. 1996 Nov 15;15(22):6311–6320. [PMC free article] [PubMed] [Google Scholar]
  21. Erickson F. L., Harding L. D., Dorris D. R., Hannig E. M. Functional analysis of homologs of translation initiation factor 2gamma in yeast. Mol Gen Genet. 1997 Feb 27;253(6):711–719. doi: 10.1007/s004380050375. [DOI] [PubMed] [Google Scholar]
  22. Ernst H., Duncan R. F., Hershey J. W. Cloning and sequencing of complementary DNAs encoding the alpha-subunit of translational initiation factor eIF-2. Characterization of the protein and its messenger RNA. J Biol Chem. 1987 Jan 25;262(3):1206–1212. [PubMed] [Google Scholar]
  23. Fabian J. R., Kimball S. R., Heinzinger N. K., Jefferson L. S. Subunit assembly and guanine nucleotide exchange activity of eukaryotic initiation factor-2B expressed in Sf9 cells. J Biol Chem. 1997 May 9;272(19):12359–12365. doi: 10.1074/jbc.272.19.12359. [DOI] [PubMed] [Google Scholar]
  24. Gallie D. R., Le H., Caldwell C., Tanguay R. L., Hoang N. X., Browning K. S. The phosphorylation state of translation initiation factors is regulated developmentally and following heat shock in wheat. J Biol Chem. 1997 Jan 10;272(2):1046–1053. doi: 10.1074/jbc.272.2.1046. [DOI] [PubMed] [Google Scholar]
  25. Gaspar N. J., Kinzy T. G., Scherer B. J., Hümbelin M., Hershey J. W., Merrick W. C. Translation initiation factor eIF-2. Cloning and expression of the human cDNA encoding the gamma-subunit. J Biol Chem. 1994 Feb 4;269(5):3415–3422. [PubMed] [Google Scholar]
  26. Gietz R. D., Sugino A. New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites. Gene. 1988 Dec 30;74(2):527–534. doi: 10.1016/0378-1119(88)90185-0. [DOI] [PubMed] [Google Scholar]
  27. Gomez E., Pavitt G. D. Identification of domains and residues within the epsilon subunit of eukaryotic translation initiation factor 2B (eIF2Bepsilon) required for guanine nucleotide exchange reveals a novel activation function promoted by eIF2B complex formation. Mol Cell Biol. 2000 Jun;20(11):3965–3976. doi: 10.1128/mcb.20.11.3965-3976.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Grosshans H., Hurt E., Simos G. An aminoacylation-dependent nuclear tRNA export pathway in yeast. Genes Dev. 2000 Apr 1;14(7):830–840. [PMC free article] [PubMed] [Google Scholar]
  29. Hannig E. M., Cigan A. M., Freeman B. A., Kinzy T. G. GCD11, a negative regulator of GCN4 expression, encodes the gamma subunit of eIF-2 in Saccharomyces cerevisiae. Mol Cell Biol. 1993 Jan;13(1):506–520. doi: 10.1128/mcb.13.1.506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Hannig E. M., Williams N. P., Wek R. C., Hinnebusch A. G. The translational activator GCN3 functions downstream from GCN1 and GCN2 in the regulatory pathway that couples GCN4 expression to amino acid availability in Saccharomyces cerevisiae. Genetics. 1990 Nov;126(3):549–562. doi: 10.1093/genetics/126.3.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Hannig E. M., Williams N. P., Wek R. C., Hinnebusch A. G. The translational activator GCN3 functions downstream from GCN1 and GCN2 in the regulatory pathway that couples GCN4 expression to amino acid availability in Saccharomyces cerevisiae. Genetics. 1990 Nov;126(3):549–562. doi: 10.1093/genetics/126.3.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Hellmuth K., Lau D. M., Bischoff F. R., Künzler M., Hurt E., Simos G. Yeast Los1p has properties of an exportin-like nucleocytoplasmic transport factor for tRNA. Mol Cell Biol. 1998 Nov;18(11):6374–6386. doi: 10.1128/mcb.18.11.6374. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Hershey J. W. Translational control in mammalian cells. Annu Rev Biochem. 1991;60:717–755. doi: 10.1146/annurev.bi.60.070191.003441. [DOI] [PubMed] [Google Scholar]
  34. Hill D. E., Struhl K. Molecular characterization of GCD1, a yeast gene required for general control of amino acid biosynthesis and cell-cycle initiation. Nucleic Acids Res. 1988 Oct 11;16(19):9253–9265. doi: 10.1093/nar/16.19.9253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Kimball S. R., Fabian J. R., Pavitt G. D., Hinnebusch A. G., Jefferson L. S. Regulation of guanine nucleotide exchange through phosphorylation of eukaryotic initiation factor eIF2alpha. Role of the alpha- and delta-subunits of eiF2b. J Biol Chem. 1998 May 22;273(21):12841–12845. doi: 10.1074/jbc.273.21.12841. [DOI] [PubMed] [Google Scholar]
  36. Kimball S. R., Jefferson L. S. Mechanisms of translational control in liver and skeletal muscle. Biochimie. 1994;76(8):729–736. doi: 10.1016/0300-9084(94)90077-9. [DOI] [PubMed] [Google Scholar]
  37. Manchester K. L., Stasikowski P. Kinetic parameters governing the formation of eIF-2.methionyl-tRNAi complexes in protein synthesis. Biochem Int. 1990;20(2):257–265. [PubMed] [Google Scholar]
  38. Marton M. J., Crouch D., Hinnebusch A. G. GCN1, a translational activator of GCN4 in Saccharomyces cerevisiae, is required for phosphorylation of eukaryotic translation initiation factor 2 by protein kinase GCN2. Mol Cell Biol. 1993 Jun;13(6):3541–3556. doi: 10.1128/mcb.13.6.3541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Matts R. L., Thomas N. S., Hurst R., London I. M. Correlation between the distribution of the reversing factor and eukaryotic initiation factor 2 in heme-deficient or double-stranded RNA-inhibited reticulocyte lysates. FEBS Lett. 1988 Aug 15;236(1):179–184. doi: 10.1016/0014-5793(88)80310-7. [DOI] [PubMed] [Google Scholar]
  40. Merrick W. C. Mechanism and regulation of eukaryotic protein synthesis. Microbiol Rev. 1992 Jun;56(2):291–315. doi: 10.1128/mr.56.2.291-315.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Meurs E. F., Galabru J., Barber G. N., Katze M. G., Hovanessian A. G. Tumor suppressor function of the interferon-induced double-stranded RNA-activated protein kinase. Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):232–236. doi: 10.1073/pnas.90.1.232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Mueller P. P., Grueter P., Hinnebusch A. G., Trachsel H. A ribosomal protein is required for translational regulation of GCN4 mRNA. Evidence for involvement of the ribosome in eIF2 recycling. J Biol Chem. 1998 Dec 4;273(49):32870–32877. doi: 10.1074/jbc.273.49.32870. [DOI] [PubMed] [Google Scholar]
  43. Nika J., Rippel S., Hannig E. M. Biochemical analysis of the eIF2beta gamma complex reveals a structural function for eIF2alpha in catalyzed nucleotide exchange. J Biol Chem. 2001 Jan 12;276(2):1051–1056. doi: 10.1074/jbc.M007398200. [DOI] [PubMed] [Google Scholar]
  44. Paddon C. J., Hannig E. M., Hinnebusch A. G. Amino acid sequence similarity between GCN3 and GCD2, positive and negative translational regulators of GCN4: evidence for antagonism by competition. Genetics. 1989 Jul;122(3):551–559. doi: 10.1093/genetics/122.3.551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Pain V. M. Initiation of protein synthesis in eukaryotic cells. Eur J Biochem. 1996 Mar 15;236(3):747–771. doi: 10.1111/j.1432-1033.1996.00747.x. [DOI] [PubMed] [Google Scholar]
  46. Pathak V. K., Nielsen P. J., Trachsel H., Hershey J. W. Structure of the beta subunit of translational initiation factor eIF-2. Cell. 1988 Aug 26;54(5):633–639. doi: 10.1016/s0092-8674(88)80007-2. [DOI] [PubMed] [Google Scholar]
  47. Pavitt G. D., Ramaiah K. V., Kimball S. R., Hinnebusch A. G. eIF2 independently binds two distinct eIF2B subcomplexes that catalyze and regulate guanine-nucleotide exchange. Genes Dev. 1998 Feb 15;12(4):514–526. doi: 10.1101/gad.12.4.514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Pavitt G. D., Yang W., Hinnebusch A. G. Homologous segments in three subunits of the guanine nucleotide exchange factor eIF2B mediate translational regulation by phosphorylation of eIF2. Mol Cell Biol. 1997 Mar;17(3):1298–1313. doi: 10.1128/mcb.17.3.1298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Price N. T., Kimball S. R., Jefferson L. S., Proud C. G. Cloning of cDNA for the gamma-subunit of mammalian translation initiation factor 2B, the guanine nucleotide-exchange factor for eukaryotic initiation factor 2. Biochem J. 1996 Sep 1;318(Pt 2):631–636. doi: 10.1042/bj3180631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Price N. T., Mellor H., Craddock B. L., Flowers K. M., Kimball S. R., Wilmer T., Jefferson L. S., Proud C. G. eIF2B, the guanine nucleotide-exchange factor for eukaryotic initiation factor 2. Sequence conservation between the alpha, beta and delta subunits of eIF2B from mammals and yeast. Biochem J. 1996 Sep 1;318(Pt 2):637–643. doi: 10.1042/bj3180637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Price N., Proud C. The guanine nucleotide-exchange factor, eIF-2B. Biochimie. 1994;76(8):748–760. doi: 10.1016/0300-9084(94)90079-5. [DOI] [PubMed] [Google Scholar]
  52. Qu S., Perlaky S. E., Organ E. L., Crawford D., Cavener D. R. Mutations at the Ser50 residue of translation factor eIF-2alpha dominantly affect developmental rate, body weight, and viability of Drosophila melanogaster. Gene Expr. 1997;6(6):349–360. [PMC free article] [PubMed] [Google Scholar]
  53. Ramaiah K. V., Dhindsa R. S., Chen J. J., London I. M., Levin D. Recycling and phosphorylation of eukaryotic initiation factor 2 on 60S subunits of 80S initiation complexes and polysomes. Proc Natl Acad Sci U S A. 1992 Dec 15;89(24):12063–12067. doi: 10.1073/pnas.89.24.12063. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Rhoads R. E. Regulation of eukaryotic protein synthesis by initiation factors. J Biol Chem. 1993 Feb 15;268(5):3017–3020. [PubMed] [Google Scholar]
  55. Rose M. D., Broach J. R. Cloning genes by complementation in yeast. Methods Enzymol. 1991;194:195–230. doi: 10.1016/0076-6879(91)94017-7. [DOI] [PubMed] [Google Scholar]
  56. Rowlands A. G., Panniers R., Henshaw E. C. The catalytic mechanism of guanine nucleotide exchange factor action and competitive inhibition by phosphorylated eukaryotic initiation factor 2. J Biol Chem. 1988 Apr 25;263(12):5526–5533. [PubMed] [Google Scholar]
  57. Sachs A. B., Sarnow P., Hentze M. W. Starting at the beginning, middle, and end: translation initiation in eukaryotes. Cell. 1997 Jun 13;89(6):831–838. doi: 10.1016/s0092-8674(00)80268-8. [DOI] [PubMed] [Google Scholar]
  58. Scheper G. C., Mulder J., Kleijn M., Voorma H. O., Thomas A. A., van Wijk R. Inactivation of eIF2B and phosphorylation of PHAS-I in heat-shocked rat hepatoma cells. J Biol Chem. 1997 Oct 24;272(43):26850–26856. doi: 10.1074/jbc.272.43.26850. [DOI] [PubMed] [Google Scholar]
  59. Shi Y., Vattem K. M., Sood R., An J., Liang J., Stramm L., Wek R. C. Identification and characterization of pancreatic eukaryotic initiation factor 2 alpha-subunit kinase, PEK, involved in translational control. Mol Cell Biol. 1998 Dec;18(12):7499–7509. doi: 10.1128/mcb.18.12.7499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Sikorski R. S., Hieter P. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics. 1989 May;122(1):19–27. doi: 10.1093/genetics/122.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Sood R., Porter A. C., Olsen D. A., Cavener D. R., Wek R. C. A mammalian homologue of GCN2 protein kinase important for translational control by phosphorylation of eukaryotic initiation factor-2alpha. Genetics. 2000 Feb;154(2):787–801. doi: 10.1093/genetics/154.2.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Vazquez de Aldana C. R., Dever T. E., Hinnebusch A. G. Mutations in the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2 alpha) that overcome the inhibitory effect of eIF-2 alpha phosphorylation on translation initiation. Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7215–7219. doi: 10.1073/pnas.90.15.7215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Vazquez de Aldana C. R., Hinnebusch A. G. Mutations in the GCD7 subunit of yeast guanine nucleotide exchange factor eIF-2B overcome the inhibitory effects of phosphorylated eIF-2 on translation initiation. Mol Cell Biol. 1994 May;14(5):3208–3222. doi: 10.1128/mcb.14.5.3208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Wek R. C. eIF-2 kinases: regulators of general and gene-specific translation initiation. Trends Biochem Sci. 1994 Nov;19(11):491–496. doi: 10.1016/0968-0004(94)90136-8. [DOI] [PubMed] [Google Scholar]
  65. Welsh G. I., Proud C. G. Regulation of protein synthesis in Swiss 3T3 fibroblasts. Rapid activation of the guanine-nucleotide-exchange factor by insulin and growth factors. Biochem J. 1992 May 15;284(Pt 1):19–23. doi: 10.1042/bj2840019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Yang W., Hinnebusch A. G. Identification of a regulatory subcomplex in the guanine nucleotide exchange factor eIF2B that mediates inhibition by phosphorylated eIF2. Mol Cell Biol. 1996 Nov;16(11):6603–6616. doi: 10.1128/mcb.16.11.6603. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES