Arginine methylation: An emerging regulator of protein function

被引:918
|
作者
Bedford, MT [1 ]
Richard, S
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA
[2] McGill Univ, Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Terry Fox Mol Oncol Grp, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Bloomfield Ctr Res Aging, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Oncol, Montreal, PQ H3T 1E2, Canada
[5] McGill Univ, Dept Med, Montreal, PQ H3T 1E2, Canada
关键词
D O I
10.1016/j.molcel.2005.04.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Arginine methylation is now coming out of the shadows of protein phosphorylation and entering the mainstream, largely due to the identification of the family of enzymes that lay down this modification. In addition, modification-specific antibodies and proteomic approaches have facilitated the identification of an array of substrates for the protein arginine methyl-transferases. This review describes recent insights into the molecular processes regulated by arginine methylation in normal and diseased cells.
引用
收藏
页码:263 / 272
页数:10
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