首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Linkage of two human pregnancy-specific beta 1-glycoprotein genes: one is associated with hydatidiform mole.
【2h】

Linkage of two human pregnancy-specific beta 1-glycoprotein genes: one is associated with hydatidiform mole.

机译:两个人类怀孕特定的β1-糖蛋白基因的链接:一个与葡萄胎有关。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A genomic clone containing two linked human pregnancy-specific beta 1-glycoprotein (PS beta G) genes has been isolated and characterized. The two genes are arranged in the same 5'----3' orientation; the 3' region (including the A2 and B-C exons) of the upstream gene, PSGGA, is linked to the 5' region (including the 5'/L and L/N exons) of PSGGB, the downstream gene. Depending upon the domains compared, PSGGA and PSGGB share 92-98% nucleotide and 86-95% amino acid sequence identity with PSG93, the most abundant PS beta G transcript. The 3' exon (B-C) of PSGGA contains four alternative splice sites and three polyadenylylation sites, which account for the 3' heterogeneity previously reported in the PS beta G family. Each of the predicted PSGGA-encoded proteins would have a different carboxyl terminus. PSGGB corresponds to the previously identified cDNA PSG6, which encodes proteins containing a 34-amino acid leader peptide and a 108-amino acid N domain, which is one amino acid shorter than the majority of PS beta G N domains. Additionally, the PSGGB-encoded proteins contain the cell-surface recognition tripeptide Arg-Gly-Asp, shared by several previously reported PS beta Gs as deduced from cDNA sequences. Northern blot hybridization performed with a PSGGB-specific oligonucleotide probe to the N domain revealed that PSGGB or a PSGGB-like gene encodes a major 1.7-kilobase mRNA in hydatidiform mole tissues and a major 2.0-kilobase mRNA in term placenta tissues. Moreover, the PSGGB-specific probe hybridized most strongly with mRNA from molar trophoblastic tissue, suggesting that the PSGGB-like species may be the gene preferentially expressed in gestational trophoblastic disease. Additionally, the sequence of a 2315-base-pair PS beta G cDNA (PSG95) that contains an N-A1-A2-B2-C domain arrangement is reported. The coding region of PSG95 is identical to the previously reported cDNA clones PSG1d and FL-NCA, but PSG95 contains an additional 518 and 523 base pairs in the 3' end as compared with PSG1d and FL-NCA, respectively.
机译:一个包含两个链接的人类怀孕特定的β1-糖蛋白(PS beta G)基因的基因组克隆已被分离和鉴定。两个基因以相同的5'---- 3'方向排列;上游基因PSGGA的3'区(包括A2和B-C外显子)与下游基因PSGGB的5'区(包括5'/ L和L / N外显子)相连。根据所比较的域,PSGGA和PSGGB与最丰富的PS beta G转录本PSG93共享92-98%的核苷酸和86-95%的氨基酸序列同一性。 PSGGA的3'外显子(B-C)包含四个备选剪接位点和三个聚腺苷酸位点,这解释了先前在PS beta G家族中报道的3'异质性。每个预测的PSGGA编码蛋白都将具有不同的羧基末端。 PSGGB对应于先前鉴定的cDNA PSG6,其编码包含34个氨基酸的前导肽和108个氨基酸的N结构域的蛋白质,该结构域比大多数PS beta G N结构域短一个氨基酸。此外,PSGGB编码的蛋白质还包含细胞表面识别三肽Arg-Gly-Asp,由cDNA序列推导的几个先前报道的PS beta G共有。用PSGGB特异性寡核苷酸探针对N结构域进行的Northern杂交显示,PSGGB或PSGGB样基因编码葡萄胎组织中的主要1.7碱基碱基mRNA和足月胎盘组织的主要2.0碱基碱基mRNA。此外,PSGGB特异性探针与磨牙滋养细胞组织中的mRNA最强地杂交,表明PSGGB样物种可能是妊娠滋养细胞疾病中优先表达的基因。另外,报道了包含N-A1-A2-B2-C结构域排列的2315个碱基对的PS beta G cDNA(PSG95)的序列。 PSG95的编码区与先前报道的cDNA克隆PSG1d和FL-NCA相同,但与PSG1d和FL-NCA相比,PSG95在3'端分别含有518和523个碱基对。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号