Olson P F, Salo T, Garrison K, Fessler J H
Molecular Biology Institute, University of California, Los Angeles 90024-1570.
J Cell Biochem. 1993 Mar;51(3):353-9. doi: 10.1002/jcb.240510315.
A cDNA encoding the Drosophila melanogaster acidic ribosomal protein rpA2 was cloned and sequenced. rpA2 is homologous to the Artemia salina acidic ribosomal protein eL12'. In situ hybridization to salivary gland polytene chromosomes localizes the rpA2 gene to band 21C. It is a single copy gene, with an mRNA of 0.8 kb. Two-dimensional gel electrophoresis of Drosophila ribosomal proteins followed by immuno-blotting showed that the rpA2 protein has an apparent relative mobility in SDS of 17 kD and an isoelectric point less than pH 5.0. Although the Drosophila gene rp21C may be the same as rpA2, the reported sequences differ. Comparisons of the aligned nucleotide sequences coding for the acidic ribosomal proteins rpA1 and rpA2 of Drosophila with those of other eukaryotes support the view of two separate, though closely related, groups of acidic proteins. Comparison with the Artemia homologues suggests that nucleotide identity may have been conserved by some constraint that acts in addition to the requirement for substantial similarity of amino acid sequences.
克隆并测序了编码果蝇酸性核糖体蛋白rpA2的cDNA。rpA2与卤虫酸性核糖体蛋白eL12'同源。对唾液腺多线染色体进行原位杂交,将rpA2基因定位到21C带。它是一个单拷贝基因,mRNA为0.8 kb。对果蝇核糖体蛋白进行二维凝胶电泳,然后进行免疫印迹分析,结果表明rpA2蛋白在SDS中的表观相对迁移率为17 kD,等电点小于pH 5.0。虽然果蝇基因rp21C可能与rpA2相同,但报道的序列有所不同。将果蝇酸性核糖体蛋白rpA1和rpA2的编码核苷酸序列与其他真核生物的序列进行比较,支持了酸性蛋白分为两个独立但密切相关的组的观点。与卤虫同源物的比较表明,除了氨基酸序列需要有实质性相似性外,可能还有某种限制因素使得核苷酸同一性得以保留。