Joh K, Mukai T, Yatsuki H, Hori K
Gene. 1985;39(1):17-24. doi: 10.1016/0378-1119(85)90102-7.
The nucleotide sequence of aldolase A mRNA in rat skeletal muscle was determined using recombinant cDNA clones and a cDNA synthesized by primer extension. The sequence is composed of 1343 nucleotides (nt) except for the poly(A) tail. Based on the sequence analysis we have deduced an open reading frame with 363 amino acids (aa) (Mr 39134). The sequence suggests several nt polymorphisms in the mRNA population, one of which causes an aa change. The determined sequence of rat aldolase A mRNA was compared with the published ones of rabbit aldolase A or rat aldolase B mRNAs. The homology between rat and rabbit aldolase A mRNA sequences is greater than that between rat aldolase A and B mRNA sequences. Multiple aldolase A mRNAs having different Mrs were detected in the various tissues, and appeared to be expressed in a tissue-specific manner. Further analysis suggests that differences in mRNA length are due to differences in the 5'-noncoding terminal region.
利用重组cDNA克隆和通过引物延伸合成的cDNA,测定了大鼠骨骼肌中醛缩酶A mRNA的核苷酸序列。除了聚腺苷酸尾外,该序列由1343个核苷酸(nt)组成。基于序列分析,我们推导了一个含363个氨基酸(aa)(Mr 39134)的开放阅读框。该序列表明mRNA群体中存在几种核苷酸多态性,其中一种导致氨基酸变化。将测定的大鼠醛缩酶A mRNA序列与已发表的兔醛缩酶A或大鼠醛缩酶B mRNA序列进行了比较。大鼠和兔醛缩酶A mRNA序列之间的同源性大于大鼠醛缩酶A和B mRNA序列之间的同源性。在各种组织中检测到具有不同Mr的多种醛缩酶A mRNA,并且似乎以组织特异性方式表达。进一步分析表明,mRNA长度的差异是由于5'-非编码末端区域的差异。