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转化生长因子β1对p34cdc2磷酸化和组蛋白H1激酶活性的抑制与G1/S期生长停滞相关。

Transforming growth factor beta 1 inhibition of p34cdc2 phosphorylation and histone H1 kinase activity is associated with G1/S-phase growth arrest.

作者信息

Howe P H, Draetta G, Leof E B

机构信息

Department of Cell Biology, Vanderbilt University, Nashville, Tennessee 37232.

出版信息

Mol Cell Biol. 1991 Mar;11(3):1185-94. doi: 10.1128/mcb.11.3.1185-1194.1991.

Abstract

Transforming growth factor beta 1 (TGF beta 1) is a potent inhibitor of epithelial cell proliferation. We present data which indicate that epithelial cell proliferation is inhibited when TGF beta 1 is added throughout the prereplicative G1 phase. Cultures become reversibly blocked in late G1 at the G1/S-phase boundary. The inhibitory effects of TGF beta 1 on cell growth occur in the presence of the RNA synthesis inhibitor 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole. Associated with this inhibitory effect is a decrease in the phosphorylation and histone H1 kinase activity of the p34cdc2 protein kinase. These data suggest that TGF beta 1 growth inhibition in epithelial cells involves the regulation of p34cdc2 activity at the G1/S transition.

摘要

转化生长因子β1(TGFβ1)是上皮细胞增殖的强效抑制剂。我们提供的数据表明,在整个复制前的G1期添加TGFβ1时,上皮细胞增殖受到抑制。培养物在G1晚期的G1/S期边界处发生可逆性阻滞。TGFβ1对细胞生长的抑制作用在RNA合成抑制剂5,6-二氯-1-β-D-呋喃核糖基苯并咪唑存在的情况下依然发生。与这种抑制作用相关的是p34cdc2蛋白激酶的磷酸化和组蛋白H1激酶活性降低。这些数据表明,TGFβ1对上皮细胞生长的抑制涉及G1/S期转换时p34cdc2活性的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c5/369389/26e2c28a24a4/molcellb00166-0013-a.jpg

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