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丝裂原活化蛋白激酶诱导非洲爪蟾分裂胚胎进入中期停滞。

Induction of metaphase arrest in cleaving Xenopus embryos by MAP kinase.

作者信息

Haccard O, Sarcevic B, Lewellyn A, Hartley R, Roy L, Izumi T, Erikson E, Maller J L

机构信息

Howard Hughes Medical Institute, University of Colorado School of Medicine, Denver 80262.

出版信息

Science. 1993 Nov 19;262(5137):1262-5. doi: 10.1126/science.8235656.

Abstract

The natural arrest of vertebrate unfertilized eggs in second meiotic metaphase results from the activity of cytostatic factor (CSF). The product of the c-mos(xe) proto-oncogene is thought to be a component of CSF and can induce metaphase arrest when injected into blastomeres of two-cell embryos. The c-Mos(xe) protein can directly activate the mitogen-activated protein kinase kinase (MAP kinase kinase) in vitro, leading to activation of MAP kinase. MAP kinase and c-Mos(xe) are active in unfertilized eggs and are rapidly inactivated after fertilization. Microinjection of thiophosphorylated MAP kinase into one blastomere of a two-cell embryo induced metaphase arrest similar to that induced by c-Mos(xe). However, only arrest with c-Mos(xe) was associated with activation of endogenous MAP kinase. These results indicate that active MAP kinase is a component of CSF in Xenopus and suggest that the CSF activity of c-Mos(xe) is mediated by MAP kinase.

摘要

脊椎动物未受精卵在第二次减数分裂中期的自然停滞是由细胞静止因子(CSF)的活性导致的。原癌基因c-mos(xe)的产物被认为是CSF的一个组成部分,当注入二细胞胚胎的卵裂球时可诱导中期停滞。c-Mos(xe)蛋白在体外可直接激活丝裂原活化蛋白激酶激酶(MAP激酶激酶),从而导致MAP激酶的激活。MAP激酶和c-Mos(xe)在未受精卵中具有活性,受精后迅速失活。将硫代磷酸化的MAP激酶显微注射到二细胞胚胎的一个卵裂球中可诱导与c-Mos(xe)诱导的类似的中期停滞。然而,只有c-Mos(xe)诱导的停滞与内源性MAP激酶的激活相关。这些结果表明,活性MAP激酶是非洲爪蟾中CSF的一个组成部分,并提示c-Mos(xe)的CSF活性是由MAP激酶介导的。

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