Erratum: Human RECQL1 participates in telomere maintenance (Nucleic Acids Research (2014) 42:9 (5671-5688) DOI: 10.1093/nar/gku200);Human RECQL1 participates in telomere maintenance

Nucleic Acids Research

Volumn 42, Issue 9, 2014, Pages 5671-5688

  Popuri, Venkateswarlu ^a   Hsu, Joseph ^a   Khadka, Prabhat ^a   Horvath, Kent ^a   Liu, Yie ^a   Croteau, Deborah L ^a   Bohr, Vilhelm A ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,6 DIHYDRO 5,6 DIHYDROXYTHYMINE; APHIDICOLIN; BINDING PROTEIN; GLYCOL; PROTEIN RECQL1; RECQ HELICASE; TELOMERIC REPEAT BINDING FACTOR 2; TELOMERIC SINGLE STRANDED BINDING PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; DNA REPLICATION; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME REGULATION; FLUORESCENCE IN SITU HYBRIDIZATION; HELA CELL LINE; HOLLIDAY JUNCTION; HUMAN; IMMUNOFLUORESCENCE; IMMUNOPRECIPITATION; PRIORITY JOURNAL; SISTER CHROMATID EXCHANGE; TELOMERE FRAGILITY; TELOMERE HOMEOSTASIS; TELOMERE LOSS; TELOMERE SHORTENING; U2OS CELL LINE;

ANIMALS; DNA REPLICATION; ELECTROPHORETIC MOBILITY SHIFT ASSAY; EXODEOXYRIBONUCLEASES; HELA CELLS; HUMANS; PROTEIN BINDING; PROTEIN TRANSPORT; RECQ HELICASES; TELOMERASE; TELOMERE HOMEOSTASIS; TELOMERIC REPEAT BINDING PROTEIN 2;

EID: 84901352249     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkw1217     Document Type: Erratum

References (71)

1. O'Sullivan, R.J. and Karlseder, J. (2010) Telomeres: Protecting chromosomes against genome instability.Nat. Rev. Mol. Cell Biol., 11, 171-181
2. de, L.T. (2005) Shelterin: The protein complex that shapes and safeguards human telomeres. Genes Dev., 19, 2100-2110
3. Harley, C.B., Futcher, A.B. and Greider, C.W. (1990) Telomeres shorten during ageing of human fibroblasts. Nature, 345, 458-460
4. Autexier, C. and Lue, N.F. (2006) The structure and function of telomerase reverse transcriptase. Annu. Rev. Biochem., 75, 493-517
5. Henson, J.D., Neumann, A.A., Yeager, T.R. and Reddel, R.R. (2002) Alternative lengthening of telomeres in mammalian cells. Oncogene, 21, 598-610. (Pubitemid 34146260
6. Muntoni, A., Neumann, A.A., Hills, M. and Reddel, R.R. (2009) Telomere elongation involves intra-molecular DNA replication in cells utilizing alternative lengthening of telomeres. Hum. Mol. Genet., 18, 1017-1027
7. Greider, C.W. (1999) Telomeres do D-loop-T-loop. Cell, 97, 419-422
8. Verdun, R.E. and Karlseder, J. (2007) Replication and protection of telomeres. Nature, 447, 924-931. (Pubitemid 46975759
9. Singh, D.K., Ghosh, A.K., Croteau, D.L. and Bohr, V.A. (2012) RecQ helicases in DNA double strand break repair and telomere maintenance. Mutat. Res., 736, 15-24
10. Ghosh, A.K., Rossi, M.L., Singh, D.K., Dunn, C., Ramamoorthy, M., Croteau, D.L., Liu, Y. and Bohr, V.A. (2012) RECQL4, the protein mutated in Rothmund-Thomson syndrome, functions in telomere maintenance. J. Biol. Chem., 287, 196-209
11. Lillard-Wetherell, K., Machwe, A., Langland, G.T., Combs, K.A., Behbehani, G.K., Schonberg, S.A., German, J., Turchi, J.J., Orren, D.K. and Groden, J. (2004) Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2. Hum. Mol. Genet., 13, 1919-1932
12. Machwe, A., Xiao, L. and Orren, D.K. (2004) TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA. Oncogene, 23, 149-156. (Pubitemid 38142249
13. Mendez-Bermudez, A., Hidalgo-Bravo, A., Cotton, V.E., Gravani, A., Jeyapalan, J.N. and Royle, N.J. (2012) The roles of WRN and BLM RecQ helicases in the alternative lengthening of telomeres. Nucleic Acids Res., 40, 10809-10820
14. Opresko, P.L., von, K.C., Laine, J.P., Harrigan, J., Hickson, I.D. and Bohr, V.A. (2002) Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases. J. Biol. Chem., 277, 41110-41119
15. Opresko, P.L., Otterlei, M., Graakjaer, J., Bruheim, P., Dawut, L., Kolvraa, S., May, A., Seidman, M.M. and Bohr, V.A. (2004) The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2. Mol. Cell, 14, 763-774
16. Opresko, P.L., Mason, P.A., Podell, E.R., Lei, M., Hickson, I.D., Cech, T.R. and Bohr, V.A. (2005) POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates. J. Biol. Chem., 280, 32069-32080
17. Stavropoulos, D.J., Bradshaw, P.S., Li, X., Pasic, I., Truong, K., Ikura, M., Ungrin, M. and Meyn, M.S. (2002) The Bloom syndrome helicase BLM interacts with TRF2 in ALT cells and promotes telomeric DNA synthesis. Hum. Mol. Genet., 11, 3135-3144
18. Ghosh, A., Rossi, M.L., Aulds, J., Croteau, D. and Bohr, V.A. (2009) Telomeric D-loops containing 8-oxo-2'-deoxyguanosine are preferred substrates for Werner and Bloom syndrome helicases and are bound by POT1. J. Biol. Chem., 284, 31074-31084
19. Dejardin, J. and Kingston, R.E. (2009) Purification of proteins associated with specific genomic loci. Cell, 136, 175-186
20. Kawabe, T., Tsuyama, N., Kitao, S., Nishikawa, K., Shimamoto, A., Shiratori, M., Matsumoto, T., Anno, K., Sato, T., Mitsui, Y. et al. (2000) Differential regulation of human RecQ family helicases in cell transformation and cell cycle. Oncogene, 19, 4764-4772
21. Muzzolini, L., Beuron, F., Patwardhan, A., Popuri, V., Cui, S., Niccolini, B., Rappas, M., Freemont, P.S. and Vindigni, A. (2007) Different quaternary structures of human RECQ1 are associated with its dual enzymatic activity. PLoS Biol., 5, e20
22. Pike, A.C., Shrestha, B., Popuri, V., Burgess-Brown, N., Muzzolini, L., Costantini, S., Vindigni, A. and Gileadi, O. (2009) Structure of the human RECQ1 helicase reveals a putative strand-separation pin. Proc. Natl. Acad. Sci. U.S.A., 106, 1039-1044
23. Thangavel, S., Mendoza-Maldonado, R., Tissino, E., Sidorova, J.M., Yin, J., Wang, W., Monnat, R.J. Jr, Falaschi, A. and Vindigni, A. (2010) Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation. Mol. Cell Biol., 30, 1382-1396
24. Popuri, V., Croteau, D.L., Brosh, R.M. Jr and Bohr, V.A. (2012) RECQ1 is required for cellular resistance to replication stress and catalyzes strand exchange on stalled replication fork structures. Cell Cycle, 11, 4252-4265
25. Berti, M., Chaudhuri, A.R., Thangavel, S., Gomathinayagam, S., Kenig, S., Vujanovic, M., Odreman, F., Glatter, T., Graziano, S., Mendoza-Maldonado, R. et al. (2013) Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition. Nat. Struct. Mol. Biol., 20, 347-354
26. Sharma, S. and Brosh, Jr. R.M. (2007) Human RECQ1 is a DNA damage responsive protein required for genotoxic stress resistance and suppression of sister chromatid exchanges. PLoS ONE, 2, e1297
27. Tadokoro, T., Kulikowicz, T., Dawut, L., Croteau, D.L. and Bohr, V.A. (2012) DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities. Aging (Albany. NY), 4, 417-429
28. Lei, M., Podell, E.R. and Cech, T.R. (2004) Structure of human POT1 bound to telomeric single-stranded DNA provides a model for chromosome end-protection. Nat. Struct. Mol. Biol., 11, 1223-1229
29. Ferrarelli, L.K., Popuri, V., Ghosh, A.K., Tadokoro, T., Canugovi, C., Hsu, J.K., Croteau, D.L. and Bohr, V.A. (2013) The RECQL4 protein, deficient in Rothmund-Thomson syndrome is active on telomeric D-loops containing DNA metabolism blocking lesions. DNA Repair (Amst.), 12, 518-528
30. Popuri, V., Bachrati, C.Z., Muzzolini, L., Mosedale, G., Costantini, S., Giacomini, E., Hickson, I.D. and Vindigni, A. (2008) The Human RecQ helicases, BLM and RECQ1, display distinct DNA substrate specificities. J. Biol. Chem., 283, 17766-17776
31. Loayza, D. and de, L.T. (2003) POT1 as a terminal transducer of TRF1 telomere length control. Nature, 423, 1013-1018. (Pubitemid 36806919
32. Lansdorp, P.M., Verwoerd, N.P., van de Rijke, F.M., Dragowska, V., Little, M.T., Dirks, R.W., Raap, A.K. and Tanke, H.J. (1996) Heterogeneity in telomere length of human chromosomes. Hum. Mol. Genet., 5, 685-691
33. Bailey, S.M., Brenneman, M.A. and Goodwin, E.H. (2004) Frequent recombination in telomeric DNA may extend the proliferative life of telomerase-negative cells. Nucleic Acids Res., 32, 3743-3751. (Pubitemid 39157721
34. Popuri, V., Huang, J., Ramamoorthy, M., Tadokoro, T., Croteau, D.L. and Bohr, V.A. (2013) RECQL5 plays co-operative and complementary roles with WRN syndrome helicase. Nucleic Acids Res., 41, 881-899
35. Aller, P., Rould, M.A., Hogg, M., Wallace, S.S. and Doublie, S. (2007) A structural rationale for stalling of a replicative DNA polymerase at the most common oxidative thymine lesion, thymine glycol. Proc. Natl. Acad. Sci. U.S.A., 104, 814-818. (Pubitemid 46154693
36. Xin, H., Liu, D., Wan, M., Safari, A., Kim, H., Sun, W., O'Connor, M.S. and Songyang, Z. (2007) TPP1 is a homologue of ciliate TEBP-beta and interacts with POT1 to recruit telomerase. Nature, 445, 559-562. (Pubitemid 46197638
37. Denchi, E.L. and de, L.T. (2007) Protection of telomeres through independent control of ATM and ATR by TRF2 and POT1. Nature, 448, 1068-1071. (Pubitemid 47345583
38. Hockemeyer, D., Palm, W., Else, T., Daniels, J.P., Takai, K.K., Ye, J.Z., Keegan, C.E., de, L.T. and Hammer, G.D. (2007) Telomere protection by mammalian Pot1 requires interaction with Tpp1. Nat. Struct. Mol. Biol., 14, 754-761
39. Martinez, P., Flores, J.M. and Blasco, M.A. (2012) 53BP1 deficiency combined with telomere dysfunction activates ATR-dependent DNA damage response. J. Cell Biol., 197, 283-300
40. Takai, K.K., Kibe, T., Donigian, J.R., Frescas, D. and de, L.T. (2011) Telomere protection by TPP1/POT1 requires tethering to TIN2. Mol. Cell, 44, 647-659
41. Cesare, A.J. and Reddel, R.R. (2008) Telomere uncapping and alternative lengthening of telomeres. Mech. Ageing Dev., 129, 99-108
42. Bhattacharyya, S., Sandy, A. and Groden, J. (2010) Unwinding protein complexes in ALTernative telomere maintenance. J. Cell Biochem., 109, 7-15
43. Laud, P.R., Multani, A.S., Bailey, S.M., Wu, L., Ma, J., Kingsley, C., Lebel, M., Pathak, S., DePinho, R.A. and Chang, S. (2005) Elevated telomere-Telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway. Genes Dev., 19, 2560-2570. (Pubitemid 41565976
44. Crabbe, L., Verdun, R.E., Haggblom, C.I. and Karlseder, J. (2004) Defective telomere lagging strand synthesis in cells lacking WRN helicase activity. Science, 306, 1951-1953. (Pubitemid 39627862
45. Wang, R.C., Smogorzewska, A. and de, L.T. (2004) Homologous recombination generates T-loop-sized deletions at human telomeres. Cell, 119, 355-368. (Pubitemid 39423838
46. Sfeir, A., Kosiyatrakul, S.T., Hockemeyer, D., MacRae, S.L., Karlseder, J., Schildkraut, C.L. and de, L.T. (2009) Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication. Cell, 138, 90-103
47. Fouche, N., Ozgur, S., Roy, D. and Griffith, J.D. (2006) Replication fork regression in repetitive DNAs. Nucleic Acids Res., 34, 6044-6050. (Pubitemid 44941182
48. Morrish, T.A. and Greider, C.W. (2009) Short telomeres initiate telomere recombination in primary and tumor cells. PLoS Genet., 5, e1000357
49. Nora, G.J., Buncher, N.A. and Opresko, P.L. (2010) Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase. Nucleic Acids Res., 38, 3984-3998
50. Arnoult, N., Saintome, C., Ourliac-Garnier, I., Riou, J.F. and Londono-Vallejo, A. (2009) Human POT1 is required for efficient telomere C-rich strand replication in the absence of WRN. Genes Dev., 23, 2915-2924
51. van, S.B., Smogorzewska, A. and de, L.T. (1998) TRF2 protects human telomeres from end-To-end fusions. Cell, 92, 401-413. (Pubitemid 28093017
52. Barefield, C. and Karlseder, J. (2012) The BLM helicase contributes to telomere maintenance through processing of late-replicating intermediate structures. Nucleic Acids Res., 40, 7358-7367
53. Karlseder, J., Hoke, K., Mirzoeva, O.K., Bakkenist, C., Kastan, M.B., Petrini, J.H. and de, L.T. (2004) The telomeric protein TRF2 binds the ATM kinase and can inhibit the ATM-dependent DNA damage response. PLoS Biol., 2, E240
54. Bachrati, C.Z., Borts, R.H. and Hickson, I.D. (2006) Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase. Nucleic Acids Res., 34, 2269-2279. (Pubitemid 43985665
55. Opresko, P.L., Sowd, G. and Wang, H. (2009) The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation. PLoS ONE, 4, e4825
56. Lu, X., Parvathaneni, S., Hara, T., Lal, A. and Sharma, S. (2013) Replication stress induces specific enrichment of RECQ1 at common fragile sites FRA3B and FRA16D. Mol. Cancer, 12, 29
57. Futami, K., Kumagai, E., Makino, H., Goto, H., Takagi, M., Shimamoto, A. and Furuichi, Y. (2008) Induction of mitotic cell death in cancer cells by small interference RNA suppressing the expression of RecQL1 helicase. Cancer Sci., 99, 71-80. (Pubitemid 350239033
58. Wilson, D.M. III and Thompson, L.H. (2007) Molecular mechanisms of sister-chromatid exchange. Mutat. Res., 616, 11-23
59. Londono-Vallejo, J.A., Der-Sarkissian, H., Cazes, L., Bacchetti, S. and Reddel, R.R. (2004) Alternative lengthening of telomeres is characterized by high rates of telomeric exchange. Cancer Res., 64, 2324-2327. (Pubitemid 38523881
60. von, Z.T., Petrie, J. and Kirkwood, T.B. (2003) Telomere-driven replicative senescence is a stress response. Nat. Biotechnol., 21, 229-230
61. Opresko, P.L., Fan, J., Danzy, S., Wilson, D.M. III and Bohr, V.A. (2005) Oxidative damage in telomeric DNA disrupts recognition by TRF1 and TRF2. Nucleic Acids Res., 33, 1230-1239. (Pubitemid 41439916
62. Zhu, X.D., Niedernhofer, L., Kuster, B., Mann, M., Hoeijmakers, J.H. and de, L.T. (2003) ERCC1/XPF removes the 3- overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes. Mol. Cell, 12, 1489-1498
63. Sharma, S., Phatak, P., Stortchevoi, A., Jasin, M. and Larocque, J.R. (2012) RECQ1 plays a distinct role in cellular response to oxidative DNA damage. DNA Repair (Amst.), 11, 537-549
64. Mohaghegh, P., Karow, J.K., Brosh, R.M. Jr, Bohr, V.A. and Hickson, I.D. (2001) The Bloom's andWerner's syndrome proteins are DNA structure-specific helicases. Nucleic Acids Res., 29, 2843-2849. (Pubitemid 32685049
65. Ohki, R. and Ishikawa, F. (2004) Telomere-bound TRF1 and TRF2 stall the replication fork at telomeric repeats. Nucleic Acids Res., 32, 1627-1637. (Pubitemid 38832708
66. Sharma, S., Stumpo, D.J., Balajee, A.S., Bock, C.B., Lansdorp, P.M., Brosh, R.M. Jr and Blackshear, P.J. (2007) RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability. Mol. Cell Biol., 27, 1784-1794
67. Chang, S., Multani, A.S., Cabrera, N.G., Naylor, M.L., Laud, P., Lombard, D., Pathak, S., Guarente, L. and DePinho, R.A. (2004) Essential role of limiting telomeres in the pathogenesis of Werner syndrome. Nat. Genet., 36, 877-882
68. Lansdorp, P.M. (2009) Telomeres and disease. EMBO J., 28, 2532-2540
69. Mendoza-Maldonado, R., Faoro, V., Bajpai, S., Berti, M., Odreman, F., Vindigni, M., Ius, T., Ghasemian, A., Bonin, S., Skrap, M. et al. (2011) The human RECQ1 helicase is highly expressed in glioblastoma and plays an important role in tumor cell proliferation. Mol. Cancer, 10, 83
70. Arai, A., Chano, T., Futami, K., Furuichi, Y., Ikebuchi, K., Inui, T., Tameno, H., Ochi, Y., Shimada, T., Hisa, Y. et al. (2011) RECQL1 and WRN proteins are potential therapeutic targets in head and neck squamous cell carcinoma. Cancer Res., 71, 4598-4607
71. Bai, Y. and Murnane, J.P. (2003) Telomere instability in a human tumor cell line expressing a dominant-negativeWRN protein. Hum. Genet., 113, 337-347