Phosphorylation of the retinoblastoma-related protein p130 in growth-arrested cells

被引:47
作者
Canhoto, AJ [1 ]
Chestukhin, A [1 ]
Litovchick, L [1 ]
DeCaprio, JA [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
关键词
p130; G0; growth arrest; pRb;
D O I
10.1038/sj.onc.1203893
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
The retinoblastoma family of proteins including pRB, p107 and p130 undergoes cell cycle dependent phosphorylation during the mid-G1 to S phase transition. This phosphorylation is dependent upon the activity of cyclin D/cdk4. In contrast to pRB and p107, p130 is phosphorylated during G0 and the early GT phase of the cell cycle, We observed that p130 is specifically phosphorylated on serine and threonine residues in T98G cells arrested in G0 by serum deprivation or density arrest. Identification of the phospho-serine and phosphothreonine residues revealed that most were clustered within a short co-linear region unique to p130, defined as the Loop, Deletion of the Loop region resulted in a change in the phosphorylation status of p130 under growth arrest conditions. Notably, deletion of the Loop did not affect the ability of p130 to bind to E2F-4 or SV40 Large T antigen, to induce growth arrest in Saos-2 cells, and to become hyperphosphorylated during the proliferative phase of the cell cycle. p130 undergoes specific G0 phosphorylation in a manner that distinguishes it from pRB and p107.
引用
收藏
页码:5116 / 5122
页数:7
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