人类DNA连接酶I基因(LIG1)的多态性,包括一个复杂的GT重复序列

Kenneth J Livak, Wayne A Little, Sylvia L Stack, Thomas A Patterson
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引用次数: 9

摘要

对源自HeLa细胞的人DNA连接酶I cDNA克隆进行测序,发现与已发表的序列存在两个未报道的差异:单个碱基变化和三个碱基缺失。这两种差异都在外显子6上,并通过扩增包含外显子5、内含子6和外显子6的片段来分析。第一个发现是内含子6的大小约为2.6 kb,而不是文献报道的1 kb。通过对扩增片段的序列分析,发现HeLa细胞外显子6的单碱基差异具有多态性,A/C差异为杂合性。对60个无亲缘关系个体的分析发现,每个等位基因的频率为0.5。对HeLa细胞和人胸腺的cDNA进行了引物跨外显子5/外显子6边界的延伸反应。结果表明,三碱基缺失是由于剪接变化引起的。对于HeLa和胸腺,三分之二的转录本与已发表的cDNA序列相似,三分之一的转录本具有三碱基缺失。最后,对内含子6的部分测序显示存在一个复杂的GT重复序列,该重复序列由48-50个核苷酸的多嘌呤通道组成,随后是可变数量的GT残基。整个多嘌呤束加上GTs重复三次。重复序列的检测需要开发专门的克隆和PCR条件。对一个家系的分析表明这个复杂的重复序列是多态的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymorphisms in the human DNA ligase I gene (LIG1) including a complex GT repeat

Sequencing of a human DNA ligase I cDNA clone derived from HeLa cells revealed two unreported differences with the published sequence: a single base change and a three-base deletion. Both differences are in exon 6, and were analyzed by amplifying a segment containing exon 5, intron 6, and exon 6. The first finding was that intron 6 is approximately 2.6 kb in size, not the 1 kb reported in the literature. By sequence analysis of amplified segments, the single-base difference in exon 6 was shown to be polymorphic, with HeLa cells heterozygous for the A/C difference. Analysis of 60 unrelated individuals found a frequency of 0.5 for each allele. Primer extension reactions across the exon 5/exon 6 boundary were performed on cDNA obtained from HeLa cells and human thymus. The results show that the three-base deletion is due to a variation in splicing. For both HeLa and thymus, two-thirds of the transcripts are like the published cDNA sequence and one-third have the three-base deletion. Finally, sequencing of part of intron 6 revealed the presence of a complex GT repeat consisting of a 48–50 nucleotide polypurine tract followed by a variable number of GT residues. This entire unit of polypurine tract plus GTs is repeated three times. Detection of the repeated sequences required the development of specialized cloning and PCR conditions. Analysis of a pedigree showed that this complex repeat is polymorphic.

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