Literature DB >> 10403781

APOBEC-2, a cardiac- and skeletal muscle-specific member of the cytidine deaminase supergene family.

W Liao1, S H Hong, B H Chan, F B Rudolph, S C Clark, L Chan.   

Abstract

APOBEC-1, which mediates the editing of apolipoprotein (apo) B mRNA, is the only known member of the C (cytidine)-->U (uridine) editing enzyme subfamily of the cytidine deaminase supergene family. Here we report the cloning of APOBEC-2, another member of the subfamily. Human and mouse APOBEC-2 both contain 224 amino acid residues, and their genes are mapped to syntenic regions of human chromosome 6 (6p21) and mouse chromosome 17. By phylogenetic analysis, APOBEC-2 is shown to be evolutionarily related to APOBEC-1, and analysis of substitution rates indicates that APOBEC-2 is a much better conserved gene than APOBEC-1. APOBEC-2 mRNA and protein are expressed exclusively in heart and skeletal muscle. APOBEC-2 does not display detectable apoB mRNA editing activity. Like other editing enzymes of the cytidine deaminase superfamily, APOBEC-2 has low, but definite, intrinsic cytidine deaminase activity. The identification of APOBEC-2 indicates that APOBEC-1 is not the only member of the C-->U editing enzyme subfamily, which, like the A (adenosine)-->I (inosine) subfamily of editing enzymes, must encompass at least two and possibly more different deaminase enzymes. It suggests that the C-->U editing affecting apoB mRNA and other RNAs is not an isolated event mediated by a single enzyme but involves multiple related proteins that have evolved from a primordial gene closely related to the housekeeping enzyme cytidine deaminase. Copyright 1999 Academic Press.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10403781     DOI: 10.1006/bbrc.1999.0925

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  47 in total

Review 1.  The challenge of target sequence specificity in C-->U RNA editing.

Authors:  Nicholas O Davidson
Journal:  J Clin Invest       Date:  2002-02       Impact factor: 14.808

2.  Injury-dependent Müller glia and ganglion cell reprogramming during tissue regeneration requires Apobec2a and Apobec2b.

Authors:  Curtis Powell; Fairouz Elsaeidi; Daniel Goldman
Journal:  J Neurosci       Date:  2012-01-18       Impact factor: 6.167

3.  A novel myogenic cell line with phenotypic properties of muscle progenitors.

Authors:  Serena Zacchigna; Even K Østli; Nikola Arsic; Lucia Pattarini; Mauro Giacca; Srdjan Djurovic
Journal:  J Mol Med (Berl)       Date:  2007-10-24       Impact factor: 4.599

Review 4.  Multiple APOBEC3 restriction factors for HIV-1 and one Vif to rule them all.

Authors:  Belete A Desimmie; Krista A Delviks-Frankenberrry; Ryan C Burdick; DongFei Qi; Taisuke Izumi; Vinay K Pathak
Journal:  J Mol Biol       Date:  2013-11-02       Impact factor: 5.469

Review 5.  Epigenetic reprogramming: is deamination key to active DNA demethylation?

Authors:  Marta Teperek-Tkacz; Vincent Pasque; George Gentsch; Anne C Ferguson-Smith
Journal:  Reproduction       Date:  2011-09-12       Impact factor: 3.906

Review 6.  Transcriptome complexity in cardiac development and diseases--an expanding universe between genome and phenome.

Authors:  Chen Gao; Yibin Wang
Journal:  Circ J       Date:  2014-04-22       Impact factor: 2.993

7.  Deficiency in APOBEC2 leads to a shift in muscle fiber type, diminished body mass, and myopathy.

Authors:  Yusuke Sato; Hans Christian Probst; Ryuichi Tatsumi; Yoshihide Ikeuchi; Michael S Neuberger; Cristina Rada
Journal:  J Biol Chem       Date:  2009-12-17       Impact factor: 5.157

8.  APOBEC3B and AID have similar nuclear import mechanisms.

Authors:  Lela Lackey; Zachary L Demorest; Allison M Land; Judd F Hultquist; William L Brown; Reuben S Harris
Journal:  J Mol Biol       Date:  2012-03-23       Impact factor: 5.469

9.  Intrinsic restriction activity by AID/APOBEC family of enzymes against the mobility of retroelements.

Authors:  Atsushi Koito; Terumasa Ikeda
Journal:  Mob Genet Elements       Date:  2011-09-01

10.  Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos.

Authors:  Christelle Etard; Urmas Roostalu; Uwe Strähle
Journal:  J Cell Biol       Date:  2010-05-03       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.