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鉴定与繁殖相关的蛋白质,并对巨型虎虾 Penaeus monodon 卵巢中的蛋白质二硫键异构酶 A6 cDNA 进行特征分析。

Identification of reproduction-related proteins and characterization of the protein disulfide isomerase A6 cDNA in ovaries of the giant tiger shrimp Penaeus monodon.

机构信息

Program in Biotechnology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

Comp Biochem Physiol Part D Genomics Proteomics. 2012 Jun;7(2):180-90. doi: 10.1016/j.cbd.2012.02.003. Epub 2012 Feb 21.

Abstract

Proteomic analysis was carried out for identification of proteins functionally involved in ovarian development of the giant tiger shrimp (Penaeus monodon). A total of 335 protein spots including 183 spots from vitellogenic (stage II) and 152 spots from mature (stage IV) ovaries of intact P. monodon broodstock were examined. Of these, 75 (40.98%) and 59 (38.82%) spots significantly matched known proteins in the databases, respectively. In addition, 270 protein spots including 167 and 103 spots from respective ovarian stages of eyestalk-ablated broodstock were also characterized. A total of 95 (56.89%) and 62 (60.19%) spots matched known proteins, respectively. Among differentially expressed reproduction-related proteins, the full-length cDNA of protein disulfide isomerase A6 (PmPDIA6) was further characterized by RACE-PCR. PmPDIA6 was 1946bp in length containing an open reading frame (ORF) of 1293bp corresponding to a polypeptide of 430 amino acids. PmPDIA6 was up-regulated at stage III ovaries in intact shrimp (P<0.05). Interestingly, eyestalk ablation resulted in a lower expression level of PmPDIA6 in each stage of ovarian development compared to that of intact broodstock (P<0.05). Results in this study clearly indicated the potential of cellular proteomic studies and gene expression analysis for identification of proteins/genes differentially expressed during ovarian development of P. monodon.

摘要

蛋白质组学分析用于鉴定与斑节对虾(Penaeus monodon)卵巢发育功能相关的蛋白质。共检测到 335 个蛋白斑点,其中 183 个来自卵黄发生期(II 期),152 个来自成熟期(IV 期)的完整斑节对虾亲虾卵巢。其中,75 个(40.98%)和 59 个(38.82%)斑点分别与数据库中的已知蛋白质显著匹配。此外,还对切除眼柄亲虾卵巢各期的 270 个蛋白斑点进行了特征分析。其中,167 个和 103 个斑点分别与各自卵巢期的已知蛋白质匹配。在差异表达的生殖相关蛋白中,进一步通过 RACE-PCR 对蛋白二硫键异构酶 A6(PmPDIA6)的全长 cDNA 进行了表征。PmPDIA6 长 1946bp,含有 1293bp 的开放阅读框(ORF),对应 430 个氨基酸的多肽。在完整虾的 III 期卵巢中,PmPDIA6 上调(P<0.05)。有趣的是,与完整亲虾相比,眼柄切除导致卵巢发育各期的 PmPDIA6 表达水平降低(P<0.05)。本研究结果清楚地表明,细胞蛋白质组学研究和基因表达分析在鉴定斑节对虾卵巢发育过程中差异表达的蛋白质/基因方面具有潜力。

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