Interaction of human SUV3 RNA/DNA helicase with BLM helicase; loss of the SUV3 gene results in mouse embryonic lethality

Mechanisms of Ageing and Development

Volumn 128, Issue 11-12, 2007, Pages 609-617

  Pereira, Mandy ^a   Mason, Penelope ^b   Szczesny, Roman J ^c   Maddukuri, Leena ^c   Dziwura, Sylwia ^d   Jedrzejczak, Robert ^e   Paul, Erin ^a   Wojcik, Andrzej ^f   Dybczynska, Lien ^d   Tudek, Barbara ^c,d   Bartnik, Ewa ^c,d   Klysik, Jan ^a   Bohr, Vilhelm A ^b   Stepien, Piotr P ^c,d  

^a BROWN UNIVERSITY   (United States)

^b NATIONAL INSTITUTE ON AGING   (United States)

^c INSTITUTE OF BIOCHEMISTRY AND BIOPHYSICS   (Poland)

^d UNIVERSITY OF WARSAW   (Poland)

^e ARGONNE NATIONAL LABORATORY   (United States)

^f INSTITUTE OF NUCLEAR CHEMISTRY AND TECHNOLOGY   (Poland)

Author keywords

BLM; Helicase; Mouse; SCE; SUV3; WRN

Indexed keywords

HELICASE; PROTEIN SUV3; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL CULTURE; CELL NUCLEUS; CONTROLLED STUDY; EMBRYOPATHY; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; GENE EXPRESSION REGULATION; GENE FREQUENCY; GENE FUNCTION; GENE INTERACTION; GENE LOSS; GENE SEQUENCE; GENOME; GENOTYPE; HELA CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; MALE; MITOSIS; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN PURIFICATION;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; DEAD-BOX RNA HELICASES; DNA HELICASES; EMBRYO LOSS; EMBRYONIC STEM CELLS; GENE SILENCING; GESTATIONAL AGE; HELA CELLS; HUMANS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MITOSIS; MOLECULAR SEQUENCE DATA; PROTEIN BINDING; RECQ HELICASES; RNA INTERFERENCE; RNA, SMALL INTERFERING; SISTER CHROMATID EXCHANGE; TRANSFECTION;

EUKARYOTA; MAMMALIA; MUS;

EID: 37349107091     PISSN: 00476374     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mad.2007.09.001     Document Type: Article

References (41)

1. Adams D.J., Biggs P.J., Cox T., Davies R., van der Weyden L., Jonkers J., Smith J., Plumb B., Taylor R., Nishijima I., Yu Y., Rogers J., and Bradley A. Mutagenic insertion and chromosome engineering resource (MICER). Nat. Genet. 36 (2004) 867-871
2. Bader J.S. Greedily building protein networks with confidence. Bioinformatics 3 (2003) 4781-4790
3. Brosch Jr. R.M., Li J.L., Kenny M.R., Karow J.K., Cooper M.P., Kureekattil R.P., Hickson I.D., and Bohr V.A. Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity. J. Biol. Chem. 275 (2000) 23500-23508
4. Chaganti R.S., Schonberg S., and German J. A manifold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. Proc. Natl. Acad. Sci. U.S.A. 71 (1974) 4508-4512
5. Dmochowska A., Stankiewicz P., Golik P., Stepien P.P., Bocian E., Hansmann I., and Bartnik E. Assignment of SUPV3L1 to human chromosome band 10q22.1 by in situ hybridization. Cytogenet. Cell Genet. 83 (1998) 84-85
6. Dmochowska A., Kalita K., Krawczyk M., Golik P., Mroczek K., Lazowska J., Stepien P.P., and Bartnik E. A human putative Suv3-like RNA helicase is conserved between Rhodobacter and all eukaryotes. Acta Biochim. Pol. 46 (1999) 155-162
7. Dziembowski A., Piwowarski J., Hoser R., Minczuk M., Dmochowska A., Siep M., van der Spek H., Grivell L., and Stepien P.P. The yeast mitochondrial degradosome. Its composition, interplay between RNA helicase and RNase activities and the role in mitochondrial RNA metabolism. J. Biol. Chem. 278 (2003) 1603-1611
8. Ellis N.A. DNA helicases in inherited human disorders. Curr. Opin. Genet. Dev. 7 (1997) 354-363
9. Ellis N.A., Groden J., Ye T.Z., Straughen J., Lennon D.J., Ciocci S., Proytcheva M., and German J. The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 83 (1995) 655-666
10. Furuichi Y. Premature aging and predisposition to cancers caused by mutations in ResQ family helicases. Ann. NY Acad. Sci. 928 (2001) 121-131
11. German J. Bloom syndrome, a Mendelian prototype of somatic mutational disease. Medicine 72 (1993) 393-406
12. Helleday T. Pathways for mitotic recombination in mammalian cells. Mutat. Res. 532 (2003) 103-115
13. Ho Y., Gruhler A., Heilbut A., Bader G.D., Moore L., Adams S.L., Millar A., Taylor P., Bennett K., Boutilier K., Yang L., Wolting C., Donaldson I., Schandorff S., Shewnarane J., Vo M., Taggart J., Goudreault M., Muskat B., Alfarano A., Dewar D., Lin Z., Michalickova K., Willems A.R., Sassi H., Nielsen P.A., Rasmussen K.J., Andersen J.R., Johansen L.E., Hansen L.H., Jespersen H., Podtelejnikov A., Nielsen E., Crawford J., Poulsen V., Sorensen B.D., Matthiesen J., Hendrickson R.C., Gleeson F., Pawson T., Moran M.F., Durocher D., Mann M., Hogue C.W., Figeys D., and Tyers M. Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometry. Nature 415 (2002) 180-183
14. Hu P., Beresten S.F., van Brabant A.J., Ye T.Z., Pandolfi P.P., Johnson F.B., Guarente L., and Ellis N.A. Evidence for BLM and Topoisomerase IIIalpha interaction in genomic stability. Hum. Mol. Genet. 10 (2001) 1287-1298
15. Hu Y., Lu X., Barnes E., Yan M., Lou H., and Luo G. Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers. Mol. Cell. Biol. 25 (2005) 3431-3442
16. Karmakar P., Seki M., Kanamori M., Hashiguchi K., Ohtsuki M., Murata E., Inoue E., Tada S., Lan L., Yasui A., and Enomoto T. BLM is an early responder to DNA double-strand breaks. BBRC 348 (2006) 62-69
17. Karow J.K., Newman R.H., Freemont P.S., and Hickson I.D. Oligomeric ring structure of the Bloom's syndrome helicase. Curr. Biol. 9 (1999) 597-600
18. Kitao S.A., Shimamoto M., Goto R.W., Miller W., Smithson A., Lindor N.M., and Furuichi Y. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat. Genet. 22 (1999) 82-84
19. Klysik J., Justice M., and Bradley A. Chromosome engineering and ENU mutagenesis, their use for defining gene function. Curr. Genom. 4 (2003) 37-50
20. Klysik J., Dinh C., and Bradley A. Two new mouse chromosome 11 balancers. Genomics 83 (2004) 303-310
21. Klysik J., and Singer J.D. Mice with the enhanced green fluorescent protein gene knocked in to chromosome 11 exhibit normal transmission ratios. Biochem. Genet. 43 (2005) 321-333
22. Marusawa H., Matsuzuawa S., Welsh K., Zou H., Armstrong R., Tamm I., and Reed J.C. HBXIP functions as a cofactor in apoptosis suppression. EMBO J. 22 (2003) 2729-2740
23. McDaniel L.D., Chester N., Watson M., Borowsky A.D., Leder P., and Schultz R.A. Chromosome instability and tumor predisposition inversely correlate with BLM protein levels. DNA Repair (Amsterdam) 2 (2003) 1387-1404
24. Minczuk M., Piwowarski J., Papworth M.A., Awiszus K., Schalinski A., Dziembowski A., Dmochowska A., Bartnik E., Tokatlidis K., Stepien P.P., and Borowski P. Localisation of the human hSuv3p helicase in the mitochondrial matrix and its preferential unwinding of dsDNA. Nucleic Acids Res. 30 (2002) 5074-5086
25. Minczuk M., Mroczek S., Pawlak S.D., and Stepien P.P. Human ATP-dependent RNA/DNA helicase hSuv3p interacts with the cofactor of survivin HBXIP. FEBS J. 272 (2005) 5008-5019
26. Mohaghegh P., Karow J.K., Brosh Jr. R.M., Bohr V.A., and Hickson I.D. The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases. Nucleic Acids Res. 29 (2001) 2843-2849
27. Opresko P.L., Otterlei M., Graakjaer J., Bruheim P., Dawut L., Kolvraa S., May A., Seldman M.M., and Bohr V.A. The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2. Mol. Cell. 14 (2004) 763-774
28. Orren D.K., Brosh Jr. R.M., Nehlin J.O., Machwe A., Gray M.D., and Bohr V.A. Enzymatic and DNA binding properties of purified WRN protein, high affinity binding to single-stranded DNA but not to DNA damage induced by 4NQO. Nucleic Acids Res. 27 (1999) 3557-3566
29. Perry P., and Wolff S. New Giemsa method for the differential staining of sister chromatids. Nature 251 (1974) 156-158
30. Ralf C., Hickson I.D., and Wu L. The Bloom syndrome helicase can promote the regression of a model replication fork. J. Biol. Chem. 281 (2006) 22839-22846
31. Ramirez-Solis R., Liu P., and Bradley A. Chromosome engineering in mice. Nature 378 (1995) 720-724
32. Sen D., and Gilbert W. Formation of parallel four-stranded complexes by guanine-rich motifs in DNA and its implications for meiosis. Nature 334 (1988) 364-366
33. Sengupta S., Linke S.P., Pedeux R., Yang Q., Farnsworth J., Garfield S.H., Valerie K., Shay J.W., Ellis N.A., Wasylyk B., and Harris C.C. BLM helicase-dependent transport of p53 to sites of stalled replication forks modulates homologous recombination. EMBO J. 22 (2003) 1210-1222
34. Sharma S., Doherty K.M., and Brosh R.M. Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability. Biochem. J. 398 (2006) 319-337
35. Shu Z., Vijayakumar S., Chen C.F., Chen P.L., and Lee W.H. Purified human SUV3p exhibits multiple-substrate unwinding activity upon conformational change. Biochemistry 43 (2004) 4781-4790
36. Stepien P.P., Margossian S.P., Landsman D., and Butow R.A. The yeast nuclear gene suv3 affecting mitochondrial post-transcriptional processes encodes a putative ATP-dependent RNA helicase. Proc. Natl. Acad. Sci. U.S.A. 89 (1992) 6813-6817
37. Szczesny R.J., Obriot H., Paczkowska A., Jedrzejczak R., Dmochowska A., Bartnik E., Formstecher P., Polakowska R., and Stepien P.P. Down-regulation of human RNA/DNA helicase SUV3 induces apoptosis by a caspase- and AIF-dependent pathway. Biol. Cell. 99 (2007) 323-332
38. Tanaka T., and Masai H. Stabilization of a stalled replication fork by concerted actions of two helicases. J. Biol. Chem. 281 (2006) 3484-3493
39. Tanner N.K., and Linder P. DExD/H box RNA helicases, from generic motors to specific dissociation functions. Mol. Cell. 8 (2001) 251-262
40. Tropea J.E., Cherry S., Nallamsetty S., Bignon C., and Waugh D.S. A generic method for the production of recombinant proteins in Escherichia coli using a dual hexahistidine-maltose-binding protein affinity tag. Methods Mol. Biol. 363 (2007) 1-19
41. Yu C.E., Oshima J., Fu Y.H., Wijsman E.M., Hisama F., Alisch R., Matthews S., Nakura J., Miki T., Ouais S., Martin G.M., Mulligan J., and Schellenberg G.D. Positional cloning of the Werner's syndrome gene. Science 272 (1996) 258-262