Iyer G S, Krahe R, Goodwin L A, Doggett N A, Siciliano M J, Funanage V L, Proujansky R
Department of Clinical Science, Alfred I. duPont Institute, Wilmington, Delaware, 19899, USA.
Genomics. 1996 May 15;34(1):143-6. doi: 10.1006/geno.1996.0254.
Creatine and creatine phosphate act as a buffer system for the regeneration of ATP in tissues with fluctuating energy demands. Following reports of the cloning of a creatine transporter in rat, rabbit, and human, we cloned and sequenced a creatine transporter from a human intestinal cDNA library. PCR amplification of genomic DNAs from somatic cell hybrid panels localized two creatine transporter (CT) genes: CT1 to Xq26-q28 and CT2 to 16p11.2. Refinement of CT1 to Xq28 was confirmed by FISH. Identification of CT2 sequences in YACs and cosmid contigs that had been ordered on human chromosome 16 enabled its assignment to the proximal end of 16p11.2. Sequencing of the CT2 gene identified sequence differences between CT1 and CT2 transcripts that were utilized to determine that CT2 is expressed in testis only. CT2 is the most proximally identified gene on chromosome 16p to date. The existence of an autosomal, testis-specific form of the human creatine transporter gene suggests that creatine transporter activity is critical for normal function of spermatazoa following meiosis.
肌酸和磷酸肌酸作为一种缓冲系统,用于在能量需求波动的组织中再生三磷酸腺苷(ATP)。在大鼠、兔子和人类中克隆出肌酸转运体的报道之后,我们从人肠道cDNA文库中克隆并测序了一种肌酸转运体。来自体细胞杂种板的基因组DNA的聚合酶链反应(PCR)扩增定位了两个肌酸转运体(CT)基因:CT1定位于Xq26 - q28,CT2定位于16p11.2。荧光原位杂交(FISH)证实了CT1到Xq28的定位细化。在已按顺序排列在人类16号染色体上的酵母人工染色体(YAC)和黏粒重叠群中鉴定出CT2序列,从而将其定位到16p11.2的近端。CT2基因的测序确定了CT1和CT2转录本之间的序列差异,这些差异被用于确定CT2仅在睾丸中表达。CT2是迄今为止在16号染色体短臂上最靠近近端鉴定出的基因。人类肌酸转运体基因存在一种常染色体、睾丸特异性形式,这表明肌酸转运体活性对于减数分裂后精子的正常功能至关重要。