Zhang H B, Martin G B, Tanksley S D, Wing R A
Soil and Crop Sciences Department, Texas A&M University, College Station 77843-2123.
Mol Gen Genet. 1994 Sep 28;244(6):613-21. doi: 10.1007/BF00282751.
A map-based cloning technique for crop plants is being developed using tomato as a model system. The target gene jointless is a recessive mutation that completely suppresses the formation of flower and fruit pedicel abscission zones. Previously, the jointless locus was mapped to a 3 cM interval between the two molecular markers TG523 and RPD158. Physical mapping of the jointless region by pulsed-field gel electrophoresis demonstrated that TG523 and RPD158 reside on a 600 kb SmaI fragment. In this study, TG523 was used as a probe to screen a tomato yeast artificial chromosome (YAC) library. Six tomato YAC (TY) clones were isolated, ranging from 220 to 380 kb in size. Genetic mapping of YAC ends demonstrated that this set of overlapping YACs encompasses the jointless locus. Two YAC ends, TY159L (L indicates left end) and TY143R (R indicates right end), cosegregate with the jointless locus. Only one of the six YACs (TY142) contained single-copy DNA sequences at both ends that could be mapped. The two ends of TY142 were mapped to either side of the jointless locus, indicating that TY142 contains a contiguous 285 kb tomato DNA fragment that probably includes the jointless locus. Physical mapping of the TY142 clone revealed that TY159L and TY143R reside on a 55 kb SalI fragment. Southern blot hybridization analysis of the DNAs of tomato lines nearly isogenic for the jointless mutation has allowed localization of the target locus to a region of less than 50 kb within the TY142 clone.
目前正在开发一种以番茄为模式系统的用于作物的基于图谱的克隆技术。目标基因无节是一种隐性突变,它完全抑制花和果实梗离层区的形成。此前,无节基因座被定位在两个分子标记TG523和RPD158之间3厘摩的区间内。通过脉冲场凝胶电泳对无节区域进行物理图谱分析表明,TG523和RPD158位于一个600 kb的SmaI片段上。在本研究中,TG523被用作探针来筛选番茄酵母人工染色体(YAC)文库。分离出了6个番茄YAC(TY)克隆,大小在220至380 kb之间。YAC末端的遗传图谱分析表明,这一组重叠的YAC包含无节基因座。两个YAC末端,TY159L(L表示左端)和TY143R(R表示右端),与无节基因座共分离。6个YAC中只有一个(TY142)两端都含有可定位的单拷贝DNA序列。TY142的两端被定位在无节基因座的两侧,表明TY142包含一个连续的285 kb番茄DNA片段,可能包括无节基因座。TY142克隆的物理图谱分析表明,TY159L和TY143R位于一个55 kb的SalI片段上。对几乎是无节突变等基因的番茄品系的DNA进行Southern杂交分析,已将目标基因座定位到TY142克隆内小于50 kb的区域。