Huang H, Acuff C G, Steinhelper M E
Department of Medicine, University of Alabama at Birmingham 35294, USA.
Am J Physiol. 1996 Oct;271(4 Pt 2):H1565-75. doi: 10.1152/ajpheart.1996.271.4.H1565.
Genomic sequences encoding mouse C-type natriuretic peptide (CNP) were isolated from bacteriophage libraries and characterized by restriction enzyme and sequence analysis. The mouse CNP gene (Nppc) comprised at least two exons and one intron and included several cis-regulatory elements in the 5'-flanking sequence. The deduced amino acid sequence of mouse CNP-22 was identical to other mammalian CNPs. Analysis of allele distributions in interspecific back-cross and recombinant inbred strains assigned Nppc to chromosome 1. CNP transcripts were detected by ribonuclease protection analysis in brain, ovary, and uterus, with lower levels in testes and epididymus. Uterine CNP transcripts and protein were low in sexually immature mice and adults at estrus and increased at proestrus, but similar variations in ovarian CNP expression were not statistically significant. Atrial natriuretic peptide and B-type natriuretic peptide transcripts were not detected in mouse ovary or uterus. Thus CNP gene expression is regulated by tissue-specific and inducible mechanisms in female reproductive organs. Correlations between CNP expression and uterine fluid content suggest that CNP may regulate uterine fluid balance in mice and other mammals.
从噬菌体文库中分离出编码小鼠C型利钠肽(CNP)的基因组序列,并通过限制酶和序列分析进行了表征。小鼠CNP基因(Nppc)至少包含两个外显子和一个内含子,并且在5'侧翼序列中包含几个顺式调控元件。推导的小鼠CNP-22氨基酸序列与其他哺乳动物的CNP相同。通过种间回交和重组近交系中的等位基因分布分析,将Nppc定位于1号染色体。通过核糖核酸酶保护分析在脑、卵巢和子宫中检测到CNP转录本,在睾丸和附睾中的水平较低。性未成熟小鼠和处于发情期的成年小鼠子宫中的CNP转录本和蛋白质含量较低,在发情前期增加,但卵巢CNP表达的类似变化无统计学意义。在小鼠卵巢或子宫中未检测到心房利钠肽和B型利钠肽转录本。因此,CNP基因表达在雌性生殖器官中受组织特异性和诱导性机制调控。CNP表达与子宫液含量之间的相关性表明,CNP可能调节小鼠和其他哺乳动物的子宫液平衡。