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DCLRE1B

Introduction

DNA cross-link repair 1B protein is a protein that in humans is encoded by the DCLRE1B gene.[1]

DNA interstrand cross-links prevent strand separation, thereby physically blocking transcription, replication, and segregation of DNA. DCLRE1B is one of several evolutionarily conserved genes involved in repair of interstrand cross-links (Dronkert et al., 2000).[supplied by OMIM][1]

Function

Function

The DCLRE1B/SNM1B/Apollo protein is a repair exonuclease that digests double-stranded and single-stranded DNA with a 5’ to 3’ directionality.[2]

Using an SNM1B/Apollo knockout mouse model, evidence was obtained that SNM1B/Apollo protein is required to protect telomeres against illegitimate non-homologous end joining that can result in genomic instabilityy and consequently in multi-organ developmental failure.[3]

In a human patient with Hoyeraal-Hreidarsson syndrome, a dominant negative mutation in the SNM1B/Apollo gene was discovered.[4] This mutation hampered the proper replication of telomeres, leading to major telomeric dysfunction and cellular senescence. SNM1B/Apollo protein appears to be a crucial factor in telomere maintenance, independent of its function in repairing DNA inter-strand crosslinks.[4]

References

References

  1. ↑ 1.0 1.1 “Entrez Gene: DCLRE1B DNA cross-link repair 1B (PSO2 homolog, S. cerevisiae)”.
  2. ↑ SengerovΓ‘ B, Allerston CK, Abu M, Lee SY, Hartley J, Kiakos K, Schofield CJ, Hartley JA, Gileadi O, McHugh PJ (2012). “Characterization of the human SNM1A and SNM1B/Apollo DNA repair exonucleases”. J. Biol. Chem. 287 (31): 26254–67. doi:10.1074/jbc.M112.367243. PMCΒ 3406710. PMIDΒ 22692201.
  3. ↑ Akhter S, Lam YC, Chang S, Legerski RJ (2010). “The telomeric protein SNM1B/Apollo is required for normal cell proliferation and embryonic development”. Aging Cell. 9 (6): 1047–56. doi:10.1111/j.1474-9726.2010.00631.x. PMCΒ 3719988. PMIDΒ 20854421.
  4. ↑ 4.0 4.1 Touzot F, Callebaut I, Soulier J, Gaillard L, Azerrad C, Durandy A, Fischer A, de Villartay JP, Revy P (2010). “Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal-Hreidarsson syndrome”. Proc. Natl. Acad. Sci. U.S.A. 107 (22): 10097–102. doi:10.1073/pnas.0914918107. PMCΒ 2890423. PMIDΒ 20479256.
Further reading

Further reading