Ars2 Promotes proper replication-dependent histone mRNA 3' end formation

Molecular Cell

Volumn 45, Issue 1, 2012, Pages 87-98

  Gruber, Joshua J ^b,c   Olejniczak, Scott H ^a   Yong, Jeongsik ^c   LaRocca, Gaspare ^a   Dreyfuss, Gideon ^c   Thompson, Craig B ^a  

^a MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARS2 PROTEIN; HISTONE; MESSENGER RNA; PEPTIDES AND PROTEINS; UNCLASSIFIED DRUG;

3' UNTRANSLATED REGION; ARTICLE; CELL PROLIFERATION; CONTROLLED STUDY; GENE CONTROL; GENE EXPRESSION; HELA CELL; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; POLYADENYLATION; PROTEIN EXPRESSION; PROTEIN PROCESSING; PROTEIN PROTEIN INTERACTION; PROTEIN RNA BINDING; PROTEIN STRUCTURE;

HELA CELLS; HISTONES; HUMANS; METHYLTRANSFERASES; MICRORNAS; NUCLEAR PROTEINS; RNA 3' END PROCESSING; RNA INTERFERENCE; RNA, MESSENGER; RNA, SMALL INTERFERING;

MAMMALIA;

EID: 84855877366     PISSN: 10972765     EISSN: 10974164     Source Type: Journal    
DOI: 10.1016/j.molcel.2011.12.020     Document Type: Article

References (34)

1. Collart D., Ramsey-Ewing A., Bortell R., Lian J., Stein J., Stein G. Isolation and characterization of a cDNA from a human histone H2B gene which is reciprocally expressed in relation to replication-dependent H2B histone genes during HL60 cell differentiation. Biochemistry 1991, 30:1610-1617.
2. Collart D., Romain P.L., Huebner K., Pockwinse S., Pilapil S., Cannizzaro L.A., Lian J.B., Croce C.M., Stein J.L., Stein G.S. A human histone H2B.1 variant gene, located on chromosome 1, utilizes alternative 3' end processing. J. Cell. Biochem. 1992, 50:374-385.
3. Diribarne G., Bensaude O. 7SK RNA, a non-coding RNA regulating P-TEFb, a general transcription factor. RNA Biol. 2009, 6:122-128.
4. Dong Z., Han M.H., Fedoroff N. The RNA-binding proteins HYL1 and SE promote accurate invitro processing of pri-miRNA by DCL1. Proc. Natl. Acad. Sci. USA 2008, 105:9970-9975.
5. Edgar R., Domrachev M., Lash A.E. Gene Expression Omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 2002, 30:207-210.
6. Girardot M., Pecquet C., Boukour S., Knoops L., Ferrant A., Vainchenker W., Giraudier S., Constantinescu S.N. miR-28 is a thrombopoietin receptor targeting microRNA detected in a fraction of myeloproliferative neoplasm patient platelets. Blood 2010, 116:437-445.
7. Grigg S.P., Canales C., Hay A., Tsiantis M. SERRATE coordinates shoot meristem function and leaf axial patterning in Arabidopsis. Nature 2005, 437:1022-1026.
8. Gruber J.J., Zatechka D.S., Sabin L.R., Yong J., Lum J.J., Kong M., Zong W.X., Zhang Z., Lau C.K., Rawlings J., et al. Ars2 links the nuclear cap-binding complex to RNA interference and cell proliferation. Cell 2009, 138:328-339.
9. He L., Thomson J.M., Hemann M.T., Hernando-Monge E., Mu D., Goodson S., Powers S., Cordon-Cardo C., Lowe S.W., Hannon G.J., Hammond S.M. A microRNA polycistron as a potential human oncogene. Nature 2005, 435:828-833.
10. Kiriyama M., Kobayashi Y., Saito M., Ishikawa F., Yonehara S. Interaction of FLASH with arsenite resistance protein 2 is involved in cell cycle progression at S phase. Mol. Cell. Biol. 2009, 29:4729-4741.
11. Laubinger S., Sachsenberg T., Zeller G., Busch W., Lohmann J.U., Rätsch G., Weigel D. Dual roles of the nuclear cap-binding complex and SERRATE in pre-mRNA splicing and microRNA processing in Arabidopsis thaliana. Proc. Natl. Acad. Sci. USA 2008, 105:8795-8800.
12. Lenasi T., Peterlin B.M., Barboric M. Cap-binding protein complex links pre-mRNA capping to transcription elongation and alternative splicing through positive transcription elongation factor b (P-TEFb). J.Biol. Chem. 2011, 286:22758-22768.
13. Lobbes D., Rallapalli G., Schmidt D.D., Martin C., Clarke J. SERRATE: a new player on the plant microRNA scene. EMBO Rep. 2006, 7:1052-1058.
14. Lum J.J., Bauer D.E., Kong M., Harris M.H., Li C., Lindsten T., Thompson C.B. Growth factor regulation of autophagy and cell survival in the absence of apoptosis. Cell 2005, 120:237-248.
15. Machida S., Chen H.Y., Adam Yuan Y. Molecular insights into miRNA processing by Arabidopsis thaliana SERRATE. Nucleic Acids Res 2011, 39:7828-7836.
16. Mandal S.S., Chu C., Wada T., Handa H., Shatkin A.J., Reinberg D. Functional interactions of RNA-capping enzyme with factors that positively and negatively regulate promoter escape by RNA polymerase II. Proc. Natl. Acad. Sci. USA 2004, 101:7572-7577.
17. Marzluff W.F., Wagner E.J., Duronio R.J. Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail. Nat. Rev. Genet. 2008, 9:843-854.
18. Morlando M., Ballarino M., Gromak N., Pagano F., Bozzoni I., Proudfoot N.J. Primary microRNA transcripts are processed co-transcriptionally. Nat. Struct. Mol. Biol. 2008, 15:902-909.
19. Narita T., Yung T.M., Yamamoto J., Tsuboi Y., Tanabe H., Tanaka K., Yamaguchi Y., Handa H. NELF interacts with CBC and participates in 3' end processing of replication-dependent histone mRNAs. Mol. Cell 2007, 26:349-365.
20. Nguyen V.T., Kiss T., Michels A.A., Bensaude O. 7SK small nuclear RNA binds to and inhibits the activity of CDK9/cyclin T complexes. Nature 2001, 414:322-325.
21. O'Donnell K.A., Wentzel E.A., Zeller K.I., Dang C.V., Mendell J.T. c-Myc-regulated microRNAs modulate E2F1 expression. Nature 2005, 435:839-843.
22. Pawlicki J.M., Steitz J.A. Nuclear networking fashions pre-messenger RNA and primary microRNA transcripts for function. Trends Cell Biol. 2010, 20:52-61.
23. Pehrson J., Cole R.D. Histone H10 accumulates in growth-inhibited cultured cells. Nature 1980, 285:43-44.
24. Pirngruber J., Shchebet A., Schreiber L., Shema E., Minsky N., Chapman R.D., Eick D., Aylon Y., Oren M., Johnsen S.A. CDK9 directs H2B monoubiquitination and controls replication-dependent histone mRNA 3'-end processing. EMBO Rep. 2009, 10:894-900.
25. Rossman T.G., Wang Z. Expression cloning for arsenite-resistance resulted in isolation of tumor-suppressor fau cDNA: possible involvement of the ubiquitin system in arsenic carcinogenesis. Carcinogenesis 1999, 20:311-316.
26. Sabin L.R., Zhou R., Gruber J.J., Lukinova N., Bambina S., Berman A., Lau C.K., Thompson C.B., Cherry S. Ars2 regulates both miRNA- and siRNA- dependent silencing and suppresses RNA virus infection in Drosophila. Cell 2009, 138:340-351.
27. Saito Y., Liang G., Egger G., Friedman J.M., Chuang J.C., Coetzee G.A., Jones P.A. Specific activation of microRNA-127 with downregulation of the proto-oncogene BCL6 by chromatin-modifying drugs in human cancer cells. Cancer Cell 2006, 9:435-443.
28. Salzler H.R., Davidson J.M., Montgomery N.D., Duronio R.J. Loss of the histone pre-mRNA processing factor stem-loop binding protein in Drosophila causes genomic instability and impaired cellular proliferation. PLoS ONE 2009, 4:e8168.
29. Sullivan K.D., Mullen T.E., Marzluff W.F., Wagner E.J. Knockdown of SLBP results in nuclear retention of histone mRNA. RNA 2009, 15:459-472.
30. Wang Y., Rathinam R., Walch A., Alahari S.K. ST14 (suppression of tumorigenicity 14) gene is a target for miR-27b, and the inhibitory effect of ST14 on cell growth is independent of miR-27b regulation. J.Biol. Chem. 2009, 284:23094-23106.
31. Wilson M.D., Wang D., Wagner R., Breyssens H., Gertsenstein M., Lobe C., Lu X., Nagy A., Burke R.D., Koop B.F., Howard P.L. ARS2 is a conserved eukaryotic gene essential for early mammalian development. Mol. Cell. Biol. 2008, 28:1503-1514.
32. Yang Z., Zhu Q., Luo K., Zhou Q. The 7SK small nuclear RNA inhibits the CDK9/cyclin T1 kinase to control transcription. Nature 2001, 414:317-322.
33. Yang L., Liu Z., Lu F., Dong A., Huang H. SERRATE is a novel nuclear regulator in primary microRNA processing in Arabidopsis. Plant J. 2006, 47:841-850.
34. Yang X.C., Burch B.D., Yan Y., Marzluff W.F., Dominski Z. FLASH, a proapoptotic protein involved in activation of caspase-8, is essential for 3' end processing of histone pre-mRNAs. Mol. Cell 2009, 36:267-278.