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鲤鱼(Cyprinus carpio)中两个卵黄蛋白原基因的结构与表达分析

Structural and expression analyses of two vitellogenin genes in the carp, Cyprinus carpio.

作者信息

Kang B J, Jung J-H, Lee J M, Lim S-G, Saito H, Kim M H, Kim Y-J, Saigusa M, Han C-H

机构信息

Department of Molecular Biology, Dongeui University, Busan 614-714, Republic of Korea.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2007 Dec;148(4):445-53. doi: 10.1016/j.cbpb.2007.07.088. Epub 2007 Aug 8.

DOI:10.1016/j.cbpb.2007.07.088
PMID:17804271
Abstract

We cloned and sequenced two vitellogenin (vg) cDNAs of the carp, Cyprinus carpio, using a cDNA library constructed from estradiol-17 beta (E2)-treated livers. One was a novel, longer 5000 bp-long cDNA termed vg-B2 encoding 1624 amino acids in a single open reading frame. The other was a shorter cDNA (vg-B1), identical to that registered previously as carp vg cDNA in the international nucleotide sequence database. The deduced amino acid sequences of these two molecules were well-aligned with known vertebrate Vgs sharing common characteristics such as N-terminal lipovitellin I (LVI), phosvitin (PV) and C-terminal lipovitellin II (LVII). The novel Vg-B2 bore a highly conserved GL/ICG motif within the LVII region, in contrast to the shorter Vg-B1 that has a truncated C-terminal and lacks the beta-component within the LVII region including the GL/ICG motif. Both vg-B2 and vg-B1 genes were expressed in the livers of females and E2-injected males. Western blot analysis using anti-Vg and anti-vitellin (Vn) antisera demonstrated that both Vg-B2 and Vg-B1 were detected as polypeptides with an estimated molecular mass of 180 kDa and 160 kDa, respectively, in the blood of females and E2-injected males. The results suggest the potential utilization of these genes as sensitive xenoestrogenic markers.

摘要

我们利用从经17β-雌二醇(E2)处理的肝脏构建的cDNA文库,克隆并测序了鲤鱼(Cyprinus carpio)的两个卵黄蛋白原(vg)cDNA。其中一个是新的、长度为5000 bp的较长cDNA,称为vg-B2,在一个单一的开放阅读框中编码1624个氨基酸。另一个是较短的cDNA(vg-B1),与国际核苷酸序列数据库中先前注册的鲤鱼vg cDNA相同。这两个分子推导的氨基酸序列与已知的脊椎动物Vgs具有良好的比对,它们具有共同特征,如N端卵黄脂磷蛋白I(LVI)、卵黄高磷蛋白(PV)和C端卵黄脂磷蛋白II(LVII)。与较短的Vg-B1相比,新的Vg-B2在LVII区域内有一个高度保守的GL/ICG基序,Vg-B1的C端被截断,在包括GL/ICG基序的LVII区域内缺乏β-组分。vg-B2和vg-B1基因在雌性和注射E2的雄性肝脏中均有表达。使用抗Vg和抗卵黄蛋白(Vn)抗血清的蛋白质免疫印迹分析表明,在雌性和注射E2的雄性血液中,Vg-B2和Vg-B1均被检测为估计分子量分别为180 kDa和160 kDa的多肽。结果表明这些基因有可能用作敏感的外源性雌激素标志物。

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