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海胆胚胎中一种胶原酶样孵化酶基因的早期表达。

Early expression of a collagenase-like hatching enzyme gene in the sea urchin embryo.

作者信息

Lepage T, Gache C

机构信息

Unité de Biologie Cellulaire Marine, Centre National de la Recherche, Université de Paris VI, Villefranche-sur-Mer, France.

出版信息

EMBO J. 1990 Sep;9(9):3003-12. doi: 10.1002/j.1460-2075.1990.tb07493.x.

Abstract

The hatching enzyme is a developmentally regulated protease secreted at the blastula stage by the sea urchin embryo to digest its protective envelope. A nearly full-length cDNA clone (HE6) encoding the entire sequence of the hatching enzyme was isolated from a prehatching blastula lambda gt11 cDNA library. The 1761 bp open reading frame codes for a preprohatching enzyme with an 18 amino acid signal sequence, a 148 amino acid activation peptide and a 421 amino acid mature enzyme which has homologies with the mammalian collagenases. Transcripts of the hatching enzyme gene are not detected in the unfertilized egg, they accumulate during the cleavage stages and disappear at hatching. This transient expression results from a transcriptional control. Thus the hatching enzyme mRNA is not a maternal gene product but a transcript synthesized at a very early stage from the zygotic genome.

摘要

孵化酶是一种在囊胚期由海胆胚胎分泌的受发育调控的蛋白酶,用于消化其保护性包膜。从孵化前的囊胚λgt11 cDNA文库中分离出一个编码孵化酶完整序列的近乎全长的cDNA克隆(HE6)。1761 bp的开放阅读框编码一种前孵化酶原,其具有18个氨基酸的信号序列、148个氨基酸的激活肽和一个与哺乳动物胶原酶具有同源性的421个氨基酸的成熟酶。在未受精卵中未检测到孵化酶基因的转录本,它们在卵裂期积累并在孵化时消失。这种瞬时表达是由转录控制引起的。因此,孵化酶mRNA不是母体基因产物,而是在合子基因组非常早期阶段合成的转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ab/552018/df0ab8905b27/emboj00236-0339-a.jpg

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