Mavrothalassitis G, Tzimagiorgis G, Mitsialis A, Zannis V, Plaitakis A, Papamatheakis J, Moschonas N
Institute of Molecular Biology and Biotechnology, Research Center of Crete, Greece.
Proc Natl Acad Sci U S A. 1988 May;85(10):3494-8. doi: 10.1073/pnas.85.10.3494.
We have isolated a series of human liver cDNA clones encoding glutamate dehydrogenase. The cDNA-derived protein sequence specifies a single 558-amino acid long polypeptide including a cleavable signal sequence of 53 amino acids. Blotting analysis of RNA from human, monkey, and rabbit showed that glutamate dehydrogenase mRNA is present in various amounts in all tissues tested. Glutamate dehydrogenase mRNAs are of four sizes and are found in different ratios in different tissues; the predominant ones are approximately 3.5 and approximately 2.9 kilobases. Blot hybridization of human genomic DNA to nonoverlapping cDNA fragments revealed multiple bands, many of which hybridize with two or more probes in a manner inconsistent with the existence of a single GLUD gene. Moreover, two separate 36-base synthetic oligonucleotides corresponding to the coding region hybridize to multiple genomic fragments, confirming the existence of more than one GLUD-related gene in human.
我们分离出了一系列编码谷氨酸脱氢酶的人肝脏cDNA克隆。cDNA推导的蛋白质序列确定了一个由558个氨基酸组成的单一多肽,其中包括一个由53个氨基酸组成的可裂解信号序列。对人、猴和兔的RNA进行印迹分析表明,在所测试的所有组织中均存在不同量的谷氨酸脱氢酶mRNA。谷氨酸脱氢酶mRNA有四种大小,在不同组织中的比例不同;主要的两种约为3.5千碱基和约2.9千碱基。人基因组DNA与非重叠cDNA片段的印迹杂交显示出多条带,其中许多条带与两个或更多探针杂交的方式与单个GLUD基因的存在不一致。此外,两条分别对应于编码区的36个碱基的合成寡核苷酸与多个基因组片段杂交,证实人类中存在不止一个与GLUD相关的基因。