Bland M M
Wellcome Research laboratories, Research Triangle Park, NC 27709.
Gene. 1993 Dec 31;137(2):351-2. doi: 10.1016/0378-1119(93)90035-2.
Alternate 5' untranslated regions (UTR) of the Ca2+/calmodulin-dependent kinase-Gr cDNA were identified by sequencing of anchored reverse transcription-polymerase chain reaction (RT-PCR) products. Three alternate 5' ends of the mRNA were spliced at the same point to a common 5' UTR. A 3-kb EcoRI-BamHI genomic DNA restriction fragment containing the alternate UTR and 5' flanking sequence was characterized by sequence analysis and identification of several potential transcriptional control elements.
通过对锚定逆转录-聚合酶链反应(RT-PCR)产物进行测序,鉴定了Ca2+/钙调蛋白依赖性激酶-Gr cDNA的交替5'非翻译区(UTR)。mRNA的三个交替5'末端在同一点剪接到一个共同的5'UTR。通过序列分析和鉴定几个潜在的转录控制元件,对一个包含交替UTR和5'侧翼序列的3kb EcoRI-BamHI基因组DNA限制片段进行了表征。