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编码新型妊娠特异性糖蛋白变体的cDNA的特性分析

Characterization of cDNA encoding novel pregnancy-specific glycoprotein variants.

作者信息

Teglund S, Zhou G Q, Hammarström S

机构信息

Department of Immunology, Umeå University, Sweden.

出版信息

Biochem Biophys Res Commun. 1995 Jun 15;211(2):656-64. doi: 10.1006/bbrc.1995.1862.

Abstract

The human pregnancy-specific glycoprotein (PSG) family consists of eleven closely related molecules mainly synthesized by placental syncytiotrophoblasts and whose function(s) are unknown. They belong to the carcinoembryonic antigen (CEA) family. As a step toward understanding PSG function, we have analysed 84 PSG cDNA clones from a fetal liver library with respect to domain arrangement and PSG identity. Four novel PSG cDNAs derived from the PSG4, PSG7, PSG11, and PSG13 genes were characterized. The PSG11 and PSG13 cDNAs had novel domain arrangements: L-N-B2-C (named type III) and L-A1-B2-C (named type IV), respectively. These splice variants were also demonstrated in placenta. PSG4 cDNA had a type IIa (L-N-A1-B2-C) and PSG7 cDNA a type I (L-N-A1-A2-B2-C) domain arrangement. PSG1, PSG4, PSG5 were found at highest frequency while PSG8 and PSG12 cDNA clones were not detected.

摘要

人类妊娠特异性糖蛋白(PSG)家族由11个密切相关的分子组成,主要由胎盘合体滋养层细胞合成,其功能尚不清楚。它们属于癌胚抗原(CEA)家族。作为了解PSG功能的第一步,我们分析了来自胎儿肝脏文库的84个PSG cDNA克隆的结构域排列和PSG身份。鉴定了来自PSG4、PSG7、PSG11和PSG13基因的四个新的PSG cDNA。PSG11和PSG13 cDNA具有新的结构域排列:分别为L-N-B2-C(命名为III型)和L-A1-B2-C(命名为IV型)。这些剪接变体在胎盘中也得到了证实。PSG4 cDNA具有IIa型(L-N-A1-B2-C)结构域排列,PSG7 cDNA具有I型(L-N-A1-A2-B2-C)结构域排列。PSG1、PSG4、PSG5出现频率最高,而未检测到PSG8和PSG12 cDNA克隆。

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