Abstract
A genomic clone containing two linked human pregnancy-specific β1-glycoprotein (PSßG) 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 PSßG 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 PSßG 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 PSßG N domains. Additionally, the PSGGB-encoded proteins contain the cell-surface recognition tripeptide Arg-Gly-Asp, shared by several previously reported PSßGs 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 PSßG 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.
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Leslie, K. K., Watanabe, S., Lei, K. J., Chou, D. Y., Plouzek, C. A., Deng, H. C., … Chou, J. Y. (1990). Linkage of two human pregnancy-specific β1-glycoprotein genes: One is associated with hydatidiform mole. Proceedings of the National Academy of Sciences of the United States of America, 87(15), 5822–5826. https://doi.org/10.1073/pnas.87.15.5822
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