Arden K C, Viars C S, Weiss S, Argentin S, Nemer M
Ludwig Institute for Cancer Research, University of California San Diego 92093-0660, USA.
Genomics. 1995 Mar 20;26(2):385-9. doi: 10.1016/0888-7543(95)80225-b.
Cardiac myocytes synthesize and secrete a family of peptide hormones with potent natriuretic, diuretic, and vasodilatory properties. These peptides are derived from precursor molecules that are encoded by two different genes, the atrial natriuretic peptide precursor A (NPPA) and the B-type natriuretic peptide or natriuretic peptide precursor B (NPPB). A human genomic clone for the NPPB gene was used to determine the chromosomal location of the NPPB gene. Analysis of Southern blot hybridization to DNAs from various somatic cell hybrids and fluorescence in situ hybridization allowed assignment of the NPPB locus to human chromosome 1p36. This location coincided with that of the NPPA locus; pulsed-field gel electrophoresis placed NPPA and NPPB within 50 kb of each other. This close chromosomal linkage, together with the conserved primary sequences and structural organization of the two natriuretic peptide precursor genes, suggests that the natriuretic peptide loci may have evolved from a common ancestor gene.
心肌细胞合成并分泌一类具有强大利钠、利尿和血管舒张特性的肽类激素。这些肽源自由两个不同基因编码的前体分子,即心房利钠肽前体A(NPPA)和B型利钠肽或利钠肽前体B(NPPB)。使用NPPB基因的人类基因组克隆来确定NPPB基因的染色体定位。对来自各种体细胞杂种的DNA进行Southern印迹杂交分析以及荧光原位杂交,使得NPPB基因座被定位到人类染色体1p36。该位置与NPPA基因座的位置一致;脉冲场凝胶电泳将NPPA和NPPB定位在彼此50 kb范围内。这种紧密的染色体连锁,连同两种利钠肽前体基因保守的一级序列和结构组织,表明利钠肽基因座可能从一个共同的祖先基因进化而来。