Leslie K K, Watanabe S, Lei K J, Chou D Y, Plouzek C A, Deng H C, Torres J, Chou J Y
Human Genetics Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5822-6. doi: 10.1073/pnas.87.15.5822.
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.
已分离并鉴定出一个包含两个相连的人妊娠特异性β1-糖蛋白(PSβG)基因的基因组克隆。这两个基因按相同的5'→3'方向排列;上游基因PSGGA的3'区域(包括A2和B - C外显子)与下游基因PSGGB的5'区域(包括5'/L和L/N外显子)相连。根据所比较的结构域,PSGGA和PSGGB与最丰富的PSβG转录本PSG93的核苷酸序列同一性为92 - 98%,氨基酸序列同一性为86 - 95%。PSGGA的3'外显子(B - C)包含四个可变剪接位点和三个聚腺苷酸化位点,这解释了先前报道的PSβG家族中的3'异质性。每个预测的由PSGGA编码的蛋白质都将有一个不同的羧基末端。PSGGB对应于先前鉴定的cDNA PSG6,其编码的蛋白质包含一个34个氨基酸的前导肽和一个108个氨基酸的N结构域,该结构域比大多数PSβG的N结构域短一个氨基酸。此外,由PSGGB编码的蛋白质含有细胞表面识别三肽Arg - Gly - Asp,从cDNA序列推导可知,几个先前报道的PSβG也共享该三肽。用针对N结构域的PSGGB特异性寡核苷酸探针进行的Northern印迹杂交显示,PSGGB或一个类似PSGGB的基因在葡萄胎组织中编码一种主要的1.7千碱基mRNA,在足月胎盘组织中编码一种主要的2.0千碱基mRNA。此外,PSGGB特异性探针与来自滋养层细胞组织的mRNA杂交最强,这表明类似PSGGB的物种可能是在妊娠滋养层疾病中优先表达的基因。另外,还报道了一个包含N - A1 - A2 - B2 - C结构域排列的2315碱基对的PSβG 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'端分别额外含有518和523个碱基对。