Literature DB >> 27800608

Inosine-specific ribonuclease activity of natural variants of human endonuclease V.

Jung In Kim1, Kosuke Tohashi1, Shigenori Iwai1, Isao Kuraoka1.   

Abstract

Adenine bases in DNA, RNA, and nucleotides are deaminated during normal metabolism via hydrolytic and nitrosative reactions. In RNA, the deaminated product inosine is resolved by human endonuclease V, and mice deficient in this enzyme are cancer-prone. We have now produced, purified, and characterized naturally occurring variants of human endonuclease V (V29I, R112Q, K114R, H141Y, and D201N). We found that H141Y, but not other variants, is catalytically impaired, suggesting that individuals homozygous for H141Y may be predisposed to disease.
© 2016 Federation of European Biochemical Societies.

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Keywords:  RNA editing; endonuclease V; inosine

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Year:  2016        PMID: 27800608     DOI: 10.1002/1873-3468.12470

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  1 in total

1.  Complex alternative splicing of human Endonuclease V mRNA, but evidence for only a single protein isoform.

Authors:  Natalia Berges; Meh Sameen Nawaz; Tuva Børresdatter Dahl; Lars Hagen; Magnar Bjørås; Jon K Laerdahl; Ingrun Alseth
Journal:  PLoS One       Date:  2019-11-08       Impact factor: 3.240

  1 in total

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