Giver C R, Grosovsky A J
Environmental Toxicology Graduate Program, University of California, Riverside 92521, USA.
Genetics. 1997 Aug;146(4):1429-39. doi: 10.1093/genetics/146.4.1429.
Two polymorphic sites are located within the heterozygous TK1 locus in the human lymphoblastoid cell line TK6: an inactivating frameshift in exon 4 of the nonfunctional allele and a phenotypically silent frameshift in exon 7 of the functional allele. Through the use of these intragenic polymorphisms and microsatellite markers that flank TK1, we demonstrate that partial gene conversion accounts for 3/75 (0.04) spontaneous and 9/163 (0.06) X-ray-induced TK1- mutants, thus comprising a significant component of forward mutations at this locus. In all cases, the conversion tract is < 1 cM, rendering double exchange a remote alternate explanation for these results. Sequence analysis of full length TK1 cDNA provides rigorous exclusion of deletion events as a mechanism for generation of these allelotypes. Detailed examination of allelotypes in TK1- mutants identified two mechanisms for the generation of coincident sequence alterations that sometimes accompanied gene conversions. Mutations within the conversion tract were attributed to either error-prone gap filling synthesis during recombinational repair or mismatch repair within a heteroduplex region following branch migration. These findings suggest that a proportion of point mutations may not be targeted to sites of DNA base damage, but rather may arise as secondary consequences from the repair of DNA strand breaks.
在人淋巴母细胞系TK6的杂合TK1基因座内存在两个多态性位点:无功能等位基因外显子4中的失活移码突变以及功能等位基因外显子7中的表型沉默移码突变。通过利用这些基因内多态性以及位于TK1侧翼的微卫星标记,我们证明部分基因转换占3/75(0.04)的自发和9/163(0.06)的X射线诱导的TK1突变体,因此构成了该基因座正向突变的一个重要组成部分。在所有情况下,转换片段<1 cM,使得双重交换成为这些结果的一个不太可能的替代解释。全长TK1 cDNA的序列分析严格排除了缺失事件作为产生这些等位基因类型的机制。对TK1突变体中等位基因类型的详细检查确定了有时伴随基因转换的同时发生的序列改变产生的两种机制。转换片段内的突变归因于重组修复期间易出错的缺口填充合成或分支迁移后异源双链区域内的错配修复。这些发现表明,一部分点突变可能不是针对DNA碱基损伤位点,而是可能作为DNA链断裂修复的次要后果出现。