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斑节对虾(Litopenaeus merguiensis)中编码卵黄蛋白原的cDNA的分子特征及卵黄蛋白原mRNA表达位点

Molecular characterization of a cDNA encoding vitellogenin in the banana shrimp, Penaeus (Litopenaeus) merguiensis and sites of vitellogenin mRNA expression.

作者信息

Phiriyangkul Pharima, Utarabhand Prapaporn

机构信息

Department of Biochemistry, Faculty of Science, Prince of Songkla University, Songkla, Thailand.

出版信息

Mol Reprod Dev. 2006 Apr;73(4):410-23. doi: 10.1002/mrd.20424.

Abstract

In order to determine the primary structure of banana shrimp, Penaeus merguiensis, vitellogenin (Vg), we previously purified vitellin (Vt) from the ovaries of vitellogenic females, and chemically analyzed the N-terminal amino acid sequence of its 78 kDa subunit. In this study, a cDNA from this species encoding Vg was cloned based on the N-terminal amino acid sequence of the major 78 kDa subunit of Vt and conserved sequences of Vg/Vt from other crustacean species. The complete nucleotide sequence of Vg cDNA was achieved by RT-PCR and 5' and 3' rapid amplification of cDNA ends (RACE) approaches. The full-length Vg cDNA consisted of 7,961 nucleotides. The open reading frame of this cDNA encoding a precursor peptide was comprised of 2,586 amino acid residues, with a putative processing site, R-X-K/R-R, recognized by subtilisin-like endoproteases. The deduced amino acid sequence was obtained from the Vg cDNA and its amino acid composition showed a high similarity to that of purified Vt. The deduced primary structure, of P. merguiensis Vg was 91.4% identical to the Vg of Penaeus semisulcatus and was also related to the Vg sequences of six other crustacean species with identities that ranged from 86.9% to 36.6%. In addition, the amino acid sequences corresponding to the signal peptide, N-terminal region and C-terminal region of P. merguiensis Vg were almost identical to the same sequences of the seven other reported crustacean species. Results from RT-PCR analysis showed that Vg mRNA expression was present in both the ovary and hepatopancreas of vitellogenic females but was not detected in other tissues including muscle, heart, and intestine of females or in the hepatopancreas of mature males. These results indicate that the Vg gene may be expressed only by mature P. merguiensis females and that both the ovary and hepatopancreas are possible sites for Vg synthesis in this species of shrimp.

摘要

为了确定墨吉对虾(Penaeus merguiensis)卵黄蛋白原(Vg)的一级结构,我们之前从处于卵黄发生期的雌虾卵巢中纯化了卵黄磷蛋白(Vt),并对其78 kDa亚基的N端氨基酸序列进行了化学分析。在本研究中,基于Vt主要78 kDa亚基的N端氨基酸序列以及其他甲壳类动物物种Vg/Vt的保守序列,克隆了该物种编码Vg的cDNA。通过逆转录聚合酶链反应(RT-PCR)和cDNA末端的5'和3'快速扩增(RACE)方法获得了Vg cDNA的完整核苷酸序列。Vg cDNA全长7961个核苷酸。该编码前体肽的cDNA开放阅读框由2586个氨基酸残基组成,具有一个假定的加工位点R-X-K/R-R,可被枯草杆菌蛋白酶样内切蛋白酶识别。从Vg cDNA推导得到氨基酸序列,其氨基酸组成与纯化的Vt高度相似。墨吉对虾Vg推导的一级结构与半滑舌对虾(Penaeus semisulcatus)的Vg有91.4%的同一性,并且与其他六种甲壳类动物物种的Vg序列也相关,同一性范围从86.9%到36.6%。此外,墨吉对虾Vg对应信号肽、N端区域和C端区域的氨基酸序列与其他七种已报道的甲壳类动物物种的相同序列几乎相同。RT-PCR分析结果表明,Vg mRNA表达存在于处于卵黄发生期的雌虾的卵巢和肝胰腺中,但在雌虾的其他组织(包括肌肉、心脏和肠道)或成熟雄虾的肝胰腺中未检测到。这些结果表明,Vg基因可能仅由成熟的墨吉对虾雌虾表达,并且卵巢和肝胰腺都是该种虾中Vg合成的可能位点。

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