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PGDS 对中华绒螯蟹精子发生的潜在调节作用特征。

Characteristic of PGDS potential regulation role on spermatogenesis in the Chinese mitten crab Eriocheir sinensis.

机构信息

Scientific Observing and Experimental Station of Fishery Resources and Environment in the Changjiang River, Freshwater Fisheries Research Center, Wuxi, Shanshui Road 9, 214081, China.

Sanquan College, Xinxiang Medical University, Xinxiang, Henan 453003, China.

出版信息

Gene. 2014 Jun 15;543(2):244-52. doi: 10.1016/j.gene.2014.04.010. Epub 2014 Apr 5.

Abstract

Prostaglandin D synthase (PGDS) catalyzes the isomerization of PGH2 to produce PGD2 in the presence of sulfhydryl compounds. In this study, a full length PGDS gene comprising 1250 nucleotides from the Chinese mitten crab Eriocheir sinensis (Es-PGDS) was characterized, with a 615 bp open reading frame encoding 204 amino acid residues. Its deduced peptide has high homology with other species' PGDS protein. The Es-PGDS mRNA expression was tissue-related, with the highest expression observed in the hepatopancreas, accessory sex gland, testis and ovaries. We also detected the different stages of tissue expression and the enzyme activity for Es-PGDS in the testis and male crab hepatopancreas. The different expression patterns and its corresponding enzyme activity level indicated that PGDS is involving in the regulation of reproductive action during the period of rapid development in E. sinensis. Furthermore our research could arouse a heat debate on the PGDS reproductive function in invertebrate and further study will be needed to determine the molecular mechanism(s) linking PGDS functions to spermatogenesis and ontogenesis if this gene is to be exploited as a molecular biomarker in further studies of development.

摘要

前列腺素 D 合酶 (PGDS) 在巯基化合物存在的情况下催化 PGH2 异构化为 PGD2。在这项研究中,从中华绒螯蟹 (Eriocheir sinensis) 中鉴定出全长 PGDS 基因,全长 1250 个核苷酸,包含 615bp 的开放阅读框,编码 204 个氨基酸残基。其推导的肽与其他物种的 PGDS 蛋白具有高度同源性。Es-PGDS mRNA 的表达与组织相关,在肝胰腺、副性腺、精巢和卵巢中表达最高。我们还检测了 Es-PGDS 在精巢和雄性蟹肝胰腺中的不同发育阶段的组织表达和酶活性。不同的表达模式及其对应的酶活性水平表明,PGDS 参与了中华绒螯蟹快速发育过程中的生殖作用的调节。此外,我们的研究可能会引发关于 PGDS 在无脊椎动物生殖功能的激烈争论,如果要将该基因作为发育研究中分子生物标志物进一步研究,需要进一步研究将 PGDS 功能与精子发生和个体发生联系起来的分子机制。

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