Qian S, Zhang J Y, Kay M A, Jacobs-Lorena M
Nucleic Acids Res. 1987 Feb 11;15(3):987-1003. doi: 10.1093/nar/15.3.987.
The expression of ribosomal protein (r-protein) genes is uniquely regulated at the translational level during early development of Drosophila. Here we report results of a detailed analysis of the r-protein rpA1 gene. A cloned DNA sequence coding for rpA1 has been identified by hybrid-selected translation and amino acid composition analysis. The rpA1 gene was localized to polytene chromosome band 53CD. The nucleotide sequence of the rpA1 gene and its cDNA have been determined. rpA1 is a single copy gene and sequence comparison between the gene and its cDNA indicates that this r-protein gene is intronless. Allelic restriction site polymorphisms outside of the gene were observed, while the coding sequence is well conserved between two Drosophila strains. The protein has unusual domains rich in Ala and charged residues. The rpA1 is homologous to the "A" family of eucaryotic acidic r-proteins which are known to play a key role in the initiation and elongation steps of protein synthesis.
在果蝇的早期发育过程中,核糖体蛋白(r蛋白)基因的表达在翻译水平上受到独特的调控。在此,我们报告了对r蛋白rpA1基因的详细分析结果。通过杂交选择翻译和氨基酸组成分析,已鉴定出一个编码rpA1的克隆DNA序列。rpA1基因定位于多线染色体带53CD。已确定rpA1基因及其cDNA的核苷酸序列。rpA1是一个单拷贝基因,基因与其cDNA之间的序列比较表明,这个r蛋白基因没有内含子。在基因外部观察到等位基因限制性位点多态性,而两个果蝇品系之间的编码序列高度保守。该蛋白具有富含丙氨酸和带电荷残基的特殊结构域。rpA1与真核酸性r蛋白的“A”家族同源,已知该家族在蛋白质合成的起始和延伸步骤中起关键作用。