Alternatively spliced forms of cyclin D1 modulate entry into the cell cycle in an inverse manner

被引:112
作者
Sawa, H [1 ]
Ohshima, TA
Ukita, H
Murakami, H
Chiba, Y
Kamada, H
Hara, M
Saito, I
机构
[1] Kyorin Univ, Sch Med, Dept Neurosurg, Tokyo, Japan
[2] Kyorin Univ, Sch Med, Dept Biochem 2, Tokyo, Japan
[3] Hokuto Hosp, Obihiro, Hokkaido, Japan
关键词
cyclin D1; cell cycle regulation; transfection; FACS; Ki-67; antigen; alternative splicing;
D O I
10.1038/sj.onc.1201691
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
Alternative splicing of cyclin D1 gene mRNA has recently been demonstrated, The novel transcript shows no splicing at the downstream exon 3 boundary and encodes a protein with an altered carboxyl-terminal domain that is a cyclin D1 variant; exon 5 is not included in the coding sequence which terminates downstream of exon 4, We here produced cells that exogenously express each form of cyclin D1 and analysed their cell cycle regulation. We found that (1) alternative splicing forms of cyclin D1 modulated entry into the cell cycle in an inverse manner; (2) both splicing forms suppressed cell growth; and (3) cells overexpressing form [a] were inhibited from entry into and completion of the S phase, although form [b]-expressing cells shelved no reduction of G1- to S transition. We also found that overexpression of either cyclin D1 form up-regulated Rb gene products, suggesting that this up-regulation may be one of the causes of growth suppression in cyclin D1 overexpressing cells.
引用
收藏
页码:1701 / 1712
页数:12
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