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一种斑马鱼卵黄蛋白原基因(vg3)编码一种没有卵黄高磷蛋白结构域的新型卵黄蛋白原,可能代表一种原始脊椎动物的卵黄蛋白原基因。

A zebrafish vitellogenin gene (vg3) encodes a novel vitellogenin without a phosvitin domain and may represent a primitive vertebrate vitellogenin gene.

作者信息

Wang H, Yan T, Tan J T, Gong Z

机构信息

Department of Biological Sciences, National University of Singapore, 119260, Singapore, Singapore.

出版信息

Gene. 2000 Oct 3;256(1-2):303-10. doi: 10.1016/s0378-1119(00)00376-0.

Abstract

By analysis of zebrafish EST (expressed sequence tag) clones from an adult cDNA library, we have identified 44 clones, about 11% of the adult EST clones, encoding vitellogenins. These vitellogenin EST clones have been derived from at least seven distinct vitellogenin genes. One of the largest vitellogenin cDNA clones, vg3, and its 5' extended clone isolated by 5' RACE (rapid amplification of cDNA ends)-PCR, have been sequenced completely. The deduced complete sequence includes a predicted mature vitellogenin of 1233 amino acids and a truncated signal peptide of 18 amino acids. Interestingly, the predicted vitellogenin has no polyserine phosvitin domain. The lack of the phosvitin domain was confirmed by isolation and sequencing of the vg3 genomic region. Phylogenetic analysis indicates that the phosvitinless vitellogenin is an intermediate between invertebrate vitellogenins and all known vertebrate vitellogenins, and thus may represent a primitive vertebrate vitellogenin. Like other vitellogenins in vertebrates, the phosvitinless vitellogenin is also synthesized mainly in the liver and weakly in the intestine.

摘要

通过对来自成年斑马鱼cDNA文库的EST(表达序列标签)克隆进行分析,我们鉴定出了44个克隆,约占成年EST克隆的11%,这些克隆编码卵黄蛋白原。这些卵黄蛋白原EST克隆源自至少七个不同的卵黄蛋白原基因。其中最大的一个卵黄蛋白原cDNA克隆vg3及其通过5' RACE(cDNA末端快速扩增)-PCR分离得到的5'延伸克隆已被完全测序。推导得到的完整序列包括一个预测的由1233个氨基酸组成的成熟卵黄蛋白原和一个由18个氨基酸组成的截短信号肽。有趣的是,预测的卵黄蛋白原没有多聚丝氨酸磷蛋白结构域。通过分离和测序vg3基因组区域证实了磷蛋白结构域的缺失。系统发育分析表明,无磷蛋白的卵黄蛋白原是无脊椎动物卵黄蛋白原和所有已知脊椎动物卵黄蛋白原之间的中间类型,因此可能代表一种原始的脊椎动物卵黄蛋白原。与脊椎动物中的其他卵黄蛋白原一样,无磷蛋白的卵黄蛋白原也主要在肝脏中合成,在肠道中的合成较弱。

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