Bower D J, Errington L H, Wainwright N R, Sime C, Morris S, Clayton R M
Biochem J. 1982 Feb 1;201(2):339-44. doi: 10.1042/bj2010339.
Double-stranded complementary DNA (cDNA) sequences were prepared from day-old chick lens total polysomal RNA and inserted into the unique PstI restriction site of the plasmid pBR322. Colonies containing sequences complementary to abundant lens poly(A)-containing RNA sequences were identified by using lens 32P-labelled cDNA. Some of these clones have been characterized as containing delta-crystallin mRNA coding sequences by genomic DNA blot hybridization and RNA blot hybridizations. Hybridization of labelled DNA from such clones to RNA blots detected four size classes of delta-crystallin RNA sequences, although Southern blots indicated that there are probably only two delta-crystallin genes.
双链互补DNA(cDNA)序列是从一日龄鸡晶状体总多核糖体RNA制备而来,并插入到质粒pBR322的独特PstI限制性酶切位点。通过使用晶状体32P标记的cDNA,鉴定出含有与丰富的晶状体含poly(A) RNA序列互补的序列的菌落。通过基因组DNA印迹杂交和RNA印迹杂交,其中一些克隆已被鉴定为含有δ-晶体蛋白mRNA编码序列。来自此类克隆的标记DNA与RNA印迹的杂交检测到四种大小类别的δ-晶体蛋白RNA序列,尽管Southern印迹表明可能只有两个δ-晶体蛋白基因。