Literature DB >> 19968858

Endoribonucleases--enzymes gaining spotlight in mRNA metabolism.

Wai Ming Li1, Tavish Barnes, Chow H Lee.   

Abstract

The efficient turnover of messenger RNA represents an important mechanism that allows the cell to control gene expression. Until recently, the mechanism of mRNA decay was mainly attributed to exonucleases, comprising enzymes that degrade RNAs from the ends of the molecules. This article summarizes the endoribonucleases, comprising enzymes that cleave RNA molecules internally, which were identified in more recent years in eukaryotic mRNA metabolism. Endoribonucleases have received little attention in the past, based on the difficulty in their identification and a lack of understanding of their physiological significance. This review aims to compare the similarities and differences among this group of enzymes, as well as their known cellular functions. Despite the many differences in protein structure, and thus difficulties in identifying them based on amino acid sequence, most endoribonucleases possess essential cellular functions and have been shown to play an important role in mRNA turnover.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19968858     DOI: 10.1111/j.1742-4658.2009.07488.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  22 in total

1.  RNA structural elements determine frequency and sites of nonhomologous recombination in an animal plus-strand RNA virus.

Authors:  Sophia Austermann-Busch; Paul Becher
Journal:  J Virol       Date:  2012-04-24       Impact factor: 5.103

2.  Polymorphic toxin systems: Comprehensive characterization of trafficking modes, processing, mechanisms of action, immunity and ecology using comparative genomics.

Authors:  Dapeng Zhang; Robson F de Souza; Vivek Anantharaman; Lakshminarayan M Iyer; L Aravind
Journal:  Biol Direct       Date:  2012-06-25       Impact factor: 4.540

3.  New Strategies for Expression and Purification of Recombinant Human RNASET2 Protein in Pichia pastoris.

Authors:  Marta Lualdi; Edoardo Pedrini; Francesca Petroni; Johnny Näsman; Christer Lindqvist; Debora Scaldaferri; Roberto Taramelli; Antonio Inforzato; Francesco Acquati
Journal:  Mol Biotechnol       Date:  2015-06       Impact factor: 2.695

Review 4.  mRNA-based therapeutics--developing a new class of drugs.

Authors:  Ugur Sahin; Katalin Karikó; Özlem Türeci
Journal:  Nat Rev Drug Discov       Date:  2014-09-19       Impact factor: 84.694

5.  Structure-Mediated RNA Decay by UPF1 and G3BP1.

Authors:  Joseph W Fischer; Veronica F Busa; Yue Shao; Anthony K L Leung
Journal:  Mol Cell       Date:  2020-02-03       Impact factor: 17.970

6.  Characterization of the endoribonuclease active site of human apurinic/apyrimidinic endonuclease 1.

Authors:  Wan-Cheol Kim; Brian R Berquist; Manbir Chohan; Christopher Uy; David M Wilson; Chow H Lee
Journal:  J Mol Biol       Date:  2011-07-06       Impact factor: 5.469

7.  ADP-ribosyl-binding and hydrolase activities of the alphavirus nsP3 macrodomain are critical for initiation of virus replication.

Authors:  Rachy Abraham; Debra Hauer; Robert Lyle McPherson; Age Utt; Ilsa T Kirby; Michael S Cohen; Andres Merits; Anthony K L Leung; Diane E Griffin
Journal:  Proc Natl Acad Sci U S A       Date:  2018-10-15       Impact factor: 11.205

8.  Role of RNase MRP in viral RNA degradation and RNA recombination.

Authors:  Hannah M Jaag; Qiasheng Lu; Mark E Schmitt; Peter D Nagy
Journal:  J Virol       Date:  2010-10-20       Impact factor: 5.103

9.  An alternative route for UDP-diacylglucosamine hydrolysis in bacterial lipid A biosynthesis.

Authors:  Louis E Metzger; Christian R H Raetz
Journal:  Biochemistry       Date:  2010-08-10       Impact factor: 3.162

10.  Structure of a eukaryotic RNase III postcleavage complex reveals a double-ruler mechanism for substrate selection.

Authors:  Yu-He Liang; Mathieu Lavoie; Marc-Andre Comeau; Sherif Abou Elela; Xinhua Ji
Journal:  Mol Cell       Date:  2014-04-03       Impact factor: 17.970

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.