Roninson I B, Ingram V M
Proc Natl Acad Sci U S A. 1981 Aug;78(8):4782-5. doi: 10.1073/pnas.78.8.4782.
In order to use specific DNA probes for the study of developmentally regulated gene expression, we have prepared cDNA clones corresponding to chicken embryonic globins by inserting cDNA.mRNA hybrids into the Pst I site of the plasmid pBR322 by using poly(dG) and poly(dC) linkers. The nucleotide sequence of the insert of one clone, representing a nearly full-length copy of an embryonic beta-like globin cDNA, has been determined. The amino acid sequence of the globin encoded by this insert is identical to the sequence of embryonic rho-globin, except for four amino acid residues near the carboxy terminus. Comparison of mRNA sequences of the embryonic and adult chicken beta-globins indicates the presence of extensive deletions in the 3' untranslated region of the embryonic gene.
为了使用特定的DNA探针来研究发育调控的基因表达,我们通过使用聚(dG)和聚(dC)接头将cDNA-mRNA杂种插入质粒pBR322的Pst I位点,制备了与鸡胚胎珠蛋白相对应的cDNA克隆。已确定一个克隆的插入片段的核苷酸序列,该克隆代表胚胎β样珠蛋白cDNA的几乎全长拷贝。该插入片段编码的珠蛋白的氨基酸序列与胚胎ρ-珠蛋白的序列相同,除了羧基末端附近的四个氨基酸残基。胚胎和成年鸡β-珠蛋白的mRNA序列比较表明,胚胎基因的3'非翻译区存在广泛的缺失。