Dolan M, Dodgson J B, Engel J D
J Biol Chem. 1983 Mar 25;258(6):3983-90.
We have determined the nucleotide sequence of the adult chicken beta-globin gene locus. The structure of the adult chicken beta-globin gene is, for the most part, analogous to that of mammalian beta-globin genes thus far examined. The gene occupies 1525 nucleotides (nt) from the major cap site to the poly(A) addition site. Introns of 92 and 810 nt interrupt the coding sequence at positions corresponding to amino acid codons 30/31 and 104/105. The regions of most significant homology outside of the transcribed sequence occur within the 5'-untranslated region where the CCAAT and ATA boxes are found -74 and -30 nucleotides from the major chicken beta-globin mRNA CAP site. Using both primer-extension and mung bean nuclease mapping to localize the 5' terminus of the adult beta-globin mRNA within the transcription unit of this gene it was found that 5'-untranslated region is heterogeneous in length with termini 80 and 83 nucleotides from the translational initiation codon. In examining the transcription unit of this gene and the processing of its RNA species during maturation to mRNA, three distinct classes of beta-globin complementary nuclear RNAs are observed. One class of RNA consists of species whose size ranges from 1750 to 900 nt. These RNAs contain all or portions of the introns and are polyadenylated. Although the introns appear to be removed in a multistep fashion, a single kinetic processing pathway is not obvious. An additional processing pathway which leads to the accumulation of stable aberrant RNAs is also observed. This second class of RNA species contains first intron sequences, but lacks portions of the beta-globin coding sequence and thus is too small to become processed to functional mRNA. The third class of beta-globin complementary RNAs appear to migrate during gel electrophoresis at positions equivalent in size to RNAs of greater than gene length (2400-4500 nt), but are probably also never processed into mature mRNA.
我们已经确定了成年鸡β-珠蛋白基因座的核苷酸序列。成年鸡β-珠蛋白基因的结构在很大程度上类似于迄今为止所研究的哺乳动物β-珠蛋白基因的结构。该基因从主要帽位点到聚腺苷酸(poly(A))添加位点占据1525个核苷酸(nt)。92 nt和810 nt的内含子在对应于氨基酸密码子30/31和104/105的位置打断编码序列。转录序列之外最显著的同源区域出现在5'-非翻译区,在那里发现CCAAT盒和ATA盒距离主要鸡β-珠蛋白mRNA帽位点分别为-74和-30个核苷酸。使用引物延伸和绿豆核酸酶作图来确定成年β-珠蛋白mRNA的5'末端在该基因转录单元内的位置,发现5'-非翻译区长度不均一,其末端距离翻译起始密码子分别为80和83个核苷酸。在研究该基因的转录单元及其RNA在成熟为mRNA过程中的加工时,观察到三种不同类型的β-珠蛋白互补核RNA。一类RNA的大小范围从1750到900 nt。这些RNA包含全部或部分内含子并且被聚腺苷酸化。尽管内含子似乎以多步方式被去除,但单一的动力学加工途径并不明显。还观察到另一种导致稳定异常RNA积累的加工途径。第二类RNA物种包含第一个内含子序列,但缺少β-珠蛋白编码序列的部分,因此太小而无法被加工成功能性mRNA。第三类β-珠蛋白互补RNA在凝胶电泳中的迁移位置似乎与大于基因长度(2400 - 4500 nt)的RNA相当,但可能也从未被加工成成熟mRNA。