Ting J, Wooden S K, Kriz R, Kelleher K, Kaufman R J, Lee A S
Gene. 1987;55(1):147-52. doi: 10.1016/0378-1119(87)90258-7.
The complete nucleotide (nt) sequence encoding the hamster 78-kDa glucose-regulated protein has been determined using a cDNA plasmid p3C5. Comparison of the nucleotide sequences from rat and hamster showed a strong conservation in the coding region as well as 5'- and 3'-untranslated regions (UTRs). The relatively long (206 nt for rat) 5'UTR shares 72% sequence homology between rat and hamster in the 142 nt upstream from the ATG start codon. This conserved region contained an imperfect inverted-repeat sequence. The long 5'UTR region is capable of forming stable dyad structures. The homology within the rat and hamster protein-coding region is 93.7%, with most of the differences resulting in silent site mutations. Out of the 654 amino acids, only four changes are detected, two of which are located in the signal peptide. While the sizes of the 3'UTR are different between the two species compared, strong sequence homologies (95%) were observed throughout the entire UTRs. Also, the 3'UTR was not rich in A + T residues as found in other eukaryotic mRNAs.
利用cDNA质粒p3C5确定了编码仓鼠78-kDa葡萄糖调节蛋白的完整核苷酸(nt)序列。大鼠和仓鼠核苷酸序列的比较表明,编码区以及5'-和3'-非翻译区(UTR)具有很强的保守性。相对较长的(大鼠为206 nt)5'UTR在ATG起始密码子上游142 nt处,大鼠和仓鼠之间的序列同源性为72%。这个保守区域包含一个不完全的反向重复序列。长的5'UTR区域能够形成稳定的二分体结构。大鼠和仓鼠蛋白质编码区的同源性为93.7%,大多数差异导致同义位点突变。在654个氨基酸中,仅检测到四处变化,其中两处位于信号肽中。虽然所比较的两个物种的3'UTR大小不同,但在整个UTR中观察到很强的序列同源性(95%)。此外,3'UTR不像其他真核mRNA那样富含A+T残基。