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莫斯与细胞周期:转化表型的分子基础。

Mos and the cell cycle: the molecular basis of the transformed phenotype.

作者信息

Yew N, Strobel M, Vande Woude G F

机构信息

ABL-Basic Research Program, NCI-Frederick Cancer Research & Development Center, Maryland 21702.

出版信息

Curr Opin Genet Dev. 1993 Feb;3(1):19-25. doi: 10.1016/s0959-437x(05)80336-3.

DOI:10.1016/s0959-437x(05)80336-3
PMID:8384034
Abstract

The product of the mos proto-oncogene is a serine/threonine kinase that is expressed at high levels in germ cells. Mos is a regulator of meiotic maturation, and is required for the initiation and progression of oocyte meiotic maturation that leads to the production of unfertilized eggs. Mos is also a component of cytostatic factor, an activity that is believed to arrest oocyte maturation at meiotic metaphase II. There is evidence showing that the Mos protein is associated with tubulin in unfertilized eggs and transformed cells, raising the possibility that it is involved in the microtubular reorganization that occurs during M-phase. Inappropriate expression of its M-phase activity during interphase of the cell cycle may be responsible for its transforming activity.

摘要

mos原癌基因的产物是一种丝氨酸/苏氨酸激酶,在生殖细胞中高水平表达。Mos是减数分裂成熟的调节因子,是卵母细胞减数分裂成熟起始和进程所必需的,该进程导致未受精卵的产生。Mos也是细胞静止因子的一个组成部分,这种活性被认为可使卵母细胞成熟停滞在减数分裂中期II。有证据表明,Mos蛋白在未受精卵和转化细胞中与微管蛋白相关,这增加了它参与M期发生的微管重组的可能性。在细胞周期间期其M期活性的不适当表达可能是其转化活性的原因。

相似文献

1
Mos and the cell cycle: the molecular basis of the transformed phenotype.莫斯与细胞周期:转化表型的分子基础。
Curr Opin Genet Dev. 1993 Feb;3(1):19-25. doi: 10.1016/s0959-437x(05)80336-3.
2
Mos and the cell cycle.
Prog Cell Cycle Res. 1997;3:251-9. doi: 10.1007/978-1-4615-5371-7_20.
3
Mos is required for MAP kinase activation and is involved in microtubule organization during meiotic maturation in the mouse.在小鼠减数分裂成熟过程中,Mos是丝裂原活化蛋白激酶激活所必需的,并且参与微管组织。
Development. 1996 Mar;122(3):815-22. doi: 10.1242/dev.122.3.815.
4
Similarities between somatic cells overexpressing the mos oncogene and oocytes during meiotic interphase.在减数分裂间期,过表达mos癌基因的体细胞与卵母细胞之间的相似性。
Cell Growth Differ. 1994 Oct;5(10):1093-103.
5
Synergy between the Mos/mitogen-activated protein kinase pathway and loss of p53 function in transformation and chromosome instability.Mos/丝裂原活化蛋白激酶途径与p53功能丧失在细胞转化和染色体不稳定性中的协同作用。
Mol Cell Biol. 1997 Jan;17(1):506-18. doi: 10.1128/MCB.17.1.506.
6
Synthesis and function of Mos: the control switch of vertebrate oocyte meiosis.Mos的合成与功能:脊椎动物卵母细胞减数分裂的控制开关
Bioessays. 1997 Jan;19(1):23-8. doi: 10.1002/bies.950190106.
7
c-mos proto-oncogene product is partly degraded after release from meiotic arrest and persists during interphase in mouse zygotes.c-mos原癌基因产物在从减数分裂停滞中释放后部分降解,并在小鼠受精卵的间期持续存在。
Dev Biol. 1991 Nov;148(1):393-7. doi: 10.1016/0012-1606(91)90347-6.
8
Meiotic abnormalities of c-mos knockout mouse oocytes: activation after first meiosis or entrance into third meiotic metaphase.c-mos基因敲除小鼠卵母细胞的减数分裂异常:第一次减数分裂后激活或进入第三次减数分裂中期。
Biol Reprod. 1996 Dec;55(6):1315-24. doi: 10.1095/biolreprod55.6.1315.
9
What does Mos do in oocytes and somatic cells?Mos在卵母细胞和体细胞中起什么作用?
Bioessays. 1997 Jan;19(1):13-21. doi: 10.1002/bies.950190105.
10
Cytostatic activity develops during meiosis I in oocytes of LT/Sv mice.在LT/Sv小鼠的卵母细胞减数分裂I期间产生细胞抑制活性。
Dev Biol. 1998 Aug 15;200(2):198-211. doi: 10.1006/dbio.1998.8930.

引用本文的文献

1
Single-Cell Dynamic Analysis of Mitosis in Haploid Embryonic Stem Cells Shows the Prolonged Metaphase and Its Association with Self-diploidization.单细胞动态分析单倍体胚胎干细胞有丝分裂显示中期延长及其与自我二倍体化的关系。
Stem Cell Reports. 2017 May 9;8(5):1124-1134. doi: 10.1016/j.stemcr.2017.03.025. Epub 2017 Apr 27.
2
Oocyte-specific genes: role in fertility and infertility.卵母细胞特异性基因:在生育与不孕中的作用
J Endocrinol Invest. 2009 May;32(5):474-81. doi: 10.1007/BF03346489.
3
Mos is not required for the initiation of meiotic maturation in Xenopus oocytes.
在非洲爪蟾卵母细胞中,减数分裂成熟的起始不需要Mos。
EMBO J. 2002 Aug 1;21(15):4026-36. doi: 10.1093/emboj/cdf400.
4
Decreased proliferation of human melanoma cell lines caused by antisense RNA against translation factor eIF-4A1.针对翻译因子eIF-4A1的反义RNA导致人黑色素瘤细胞系增殖减少。
Br J Cancer. 2002 Jun 17;86(12):1957-62. doi: 10.1038/sj.bjc.6600351.
5
Kinase inhibitors in cancer therapy: a look ahead.癌症治疗中的激酶抑制剂:展望未来。
Drugs. 2000 Mar;59(3):435-76. doi: 10.2165/00003495-200059030-00004.
6
Activation of the MKK/ERK pathway during somatic cell mitosis: direct interactions of active ERK with kinetochores and regulation of the mitotic 3F3/2 phosphoantigen.体细胞有丝分裂过程中MKK/ERK通路的激活:活性ERK与动粒的直接相互作用及有丝分裂3F3/2磷酸化抗原的调控
J Cell Biol. 1998 Sep 21;142(6):1533-45. doi: 10.1083/jcb.142.6.1533.
7
Mutation analysis of the c-mos proto-oncogene in human ovarian teratomas.人卵巢畸胎瘤中c-mos原癌基因的突变分析。
Br J Cancer. 1998 May;77(10):1642-4. doi: 10.1038/bjc.1998.269.
8
Synergy between the Mos/mitogen-activated protein kinase pathway and loss of p53 function in transformation and chromosome instability.Mos/丝裂原活化蛋白激酶途径与p53功能丧失在细胞转化和染色体不稳定性中的协同作用。
Mol Cell Biol. 1997 Jan;17(1):506-18. doi: 10.1128/MCB.17.1.506.
9
Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma.甲状腺髓样癌和嗜铬细胞瘤中c-mos原癌基因及内皮素B受体基因的突变分析
Br J Cancer. 1996 Aug;74(3):339-41. doi: 10.1038/bjc.1996.363.
10
Mos oncogene product associates with kinetochores in mammalian somatic cells and disrupts mitotic progression.Mos癌基因产物与哺乳动物体细胞中的动粒相关联,并破坏有丝分裂进程。
Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8329-33. doi: 10.1073/pnas.91.18.8329.