4.6 Article

Dual recognition-incision enzymes might be involved in mismatch repair and meiosis

Journal

TRENDS IN BIOCHEMICAL SCIENCES
Volume 25, Issue 9, Pages 414-418

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/S0968-0004(00)01623-6

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Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM029009] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [GM-29009] Funding Source: Medline

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Mismatch repair in many organisms depends on three proteins: the mismatch-recognition protein MutS, a nicking endonuclease MutH, and MutL, which acts as a scaffold between these. However, many genomes lack MutL but possess MutS. In one of these cases, in a coral mitochondrial genome, a gene is present that encodes a MutS protein fused to an HNH nicking endonuclease, potentially eliminating the requirement for MutL, Likewise, many prokaryotes could operate similarly, independently of MutL by encoding a fused MutS-Smr (MutS2) protein. Smr, which is proposed to be a nicking endonuclease, can also be found separately in many eukaryotes, where it might play a role in mismatch repair or meiotic chromosome crossing-over.

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