Levine M A, Modi W S, O'Brien S J
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Genomics. 1990 Oct;8(2):380-6. doi: 10.1016/0888-7543(90)90296-7.
The signal-transducing G proteins are heterotrimers composed of three subunits, alpha, beta, and gamma. Multiple distinctive forms of the alpha, beta, and gamma subunits, each encoded by a distinct gene, have been described. To investigate further the structural diversity of the beta subunits, we recently cloned and characterized a novel cDNA encoding a third form of the G protein beta subunit, which we have termed beta 3. The protein corresponding to beta 3 has not yet been identified. The three forms of the beta subunit show 81-90% amino acid sequence identity. Previous studies had localized the human genes for the beta 1 and beta 2 subunits to chromosomes 1 and 7, respectively. The present studies were designed to determine whether the gene encoding beta 3 is linked to either the beta 1 or the beta 2 gene. Genomic DNA was isolated from a panel of rodent-human hybrid cell lines and analyzed by hybridization to cDNAs for beta 1 and beta 3. Discordancy analysis allowed assignment of the beta 3 gene to chromosome 12 and confirmed the previous assignment of the beta 1 gene to chromosome 1. These results were confirmed and extended by using in situ chromosome hybridization, which permitted the regional localization of the beta 1 gene to 1pter----p31.2 and the beta 3 gene to 12pter----p12.3. Digestion of human genomic DNA with 10 restriction enzymes failed to disclose a restriction fragment length polymorphism for the beta 3 gene. These data indicate that there is considerable diversity in the genomic organization of the beta subunit family.
信号转导G蛋白是由α、β和γ三个亚基组成的异源三聚体。已经描述了α、β和γ亚基的多种不同形式,每个亚基都由一个不同的基因编码。为了进一步研究β亚基的结构多样性,我们最近克隆并鉴定了一种编码G蛋白β亚基第三种形式的新cDNA,我们将其命名为β3。与β3对应的蛋白质尚未被鉴定出来。β亚基的三种形式显示出81 - 90%的氨基酸序列同一性。先前的研究已将人类β1和β2亚基的基因分别定位到1号和7号染色体上。本研究旨在确定编码β3的基因是否与β1或β2基因连锁。从一组啮齿动物 - 人类杂交细胞系中分离出基因组DNA,并通过与β1和β3的cDNA杂交进行分析。不一致性分析将β3基因定位到12号染色体,并证实了先前将β1基因定位到1号染色体的结果。通过使用原位染色体杂交,这些结果得到了证实和扩展,原位杂交允许将β1基因区域定位到1pter----p31.2,将β3基因区域定位到12pter----p12.3。用10种限制性内切酶消化人类基因组DNA未能揭示β3基因的限制性片段长度多态性。这些数据表明β亚基家族的基因组组织存在相当大的多样性。