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在小鼠卵母细胞减数分裂过程中,细胞周期蛋白B的积累需要c-mos基因产物。

The c-mos gene product is required for cyclin B accumulation during meiosis of mouse eggs.

作者信息

O'Keefe S J, Kiessling A A, Cooper G M

机构信息

Dana-Farber Cancer Institute, Boston, MA.

出版信息

Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7869-72. doi: 10.1073/pnas.88.17.7869.

Abstract

The c-mos protooncogene is expressed as a maternal message that is required for oocyte meiosis. The mechanism of action of c-mos was investigated by analysis of mouse eggs injected with antisense c-mos oligonucleotides. In antisense-injected eggs, maturation-promoting factor was not reactivated after the completion of meiosis I, leading to the formation of nuclei containing decondensed chromatin within 2-3 hr after polar body extrusion. This was correlated with a failure of the injected eggs to accumulate newly synthesized cyclin B. The c-mos protooncogene thus appears to affect the pathway that regulates cyclin B stability during meiosis of mouse eggs.

摘要

原癌基因c-mos作为一种母源信息表达,是卵母细胞减数分裂所必需的。通过对注射反义c-mos寡核苷酸的小鼠卵母细胞进行分析,研究了c-mos的作用机制。在注射反义寡核苷酸的卵母细胞中,减数分裂I完成后成熟促进因子未被重新激活,导致在极体排出后2-3小时内形成含有解聚染色质的细胞核。这与注射的卵母细胞未能积累新合成的细胞周期蛋白B有关。因此,原癌基因c-mos似乎影响了小鼠卵母细胞减数分裂过程中调节细胞周期蛋白B稳定性的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7173/52405/019145b62651/pnas01067-0421-a.jpg

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