Voelkel-Meiman K, Roeder G S
Department of Biology, Yale University, New Haven, Connecticut 06511-8112.
Genetics. 1990 Dec;126(4):851-67. doi: 10.1093/genetics/126.4.851.
The recombination-stimulating sequence, HOT1, corresponds to the promoter of transcription by yeast RNA polymerase I. The effect of HOT1 on mitotic interchromosomal recombination was examined in diploid strains carrying a heterozygous URA3 gene on chromosome III. The frequency of Ura- recombinants was increased 20-fold when HOT1 was inserted into the chromosome III copy marked with URA3, at a location 48 kbp centromere-proximal to URA3. Ura- recombinants were increased only 2-fold when HOT1 and URA3 were on opposite homologues. These results suggest that most HOT1-promoted Ura- recombinants result from gene conversion and that sequences on the HOT1-containing chromosome are preferentially converted. Characterization of Ura- recombinants isolated from strains carrying multiple markers on chromosome III indicates that HOT1-promoted gene conversion tracts are unusually long (often greater than 75 kbp) and almost always continuous. Furthermore, conversion tracts frequently extend to both sides of HOT1. We suggest that HOT1 promotes the formation of a double-strand break which is often followed by exonucleolytic digestion. Repair of the broken chromosome could then result from gap repair or from replicative repair primed only by the centromere-containing chromosomal fragment.
重组刺激序列HOT1与酵母RNA聚合酶I的转录启动子相对应。在第三条染色体上携带杂合URA3基因的二倍体菌株中检测了HOT1对有丝分裂染色体间重组的影响。当HOT1插入到用URA3标记的第三条染色体拷贝上、位于URA3着丝粒近端48千碱基对处时,Ura-重组体的频率增加了20倍。当HOT1和URA3位于相反的同源染色体上时,Ura-重组体仅增加了2倍。这些结果表明,大多数由HOT1促进产生的Ura-重组体是由基因转换导致的,并且含HOT1的染色体上的序列被优先转换。对从第三条染色体上携带多个标记的菌株中分离出的Ura-重组体的表征表明,由HOT1促进的基因转换片段异常长(通常大于75千碱基对)且几乎总是连续的。此外,转换片段经常延伸到HOT1的两侧。我们认为,HOT1促进了双链断裂的形成,随后常常伴随着核酸外切酶消化。断裂染色体的修复可能是由缺口修复或仅由含着丝粒的染色体片段引发的复制性修复导致的。