Segal G, Sarfatti M, Schaffer M A, Ori N, Zamir D, Fluhr R
Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel.
Mol Gen Genet. 1992 Jan;231(2):179-85. doi: 10.1007/BF00279789.
The dominant gene I2 confers on tomato (Lycopersicon esculentum) resistance against the fungus Fusarium oxysporum f. sp. lycopersici race 2. A restriction fragment length polymorphism (RFLP) marker, TG105, has recently been found to be tightly linked to I2. The potential for cloning this gene by a reverse genetics approach prompted us to describe in both genetic and physical detail the region surrounding the I2 locus on chromosome 11. We have analyzed patterns of segregation of RFLP markers on chromosome 11 and Fusarium resistance in 140 F2 plants from a cross between Fusarium-resistant and susceptible parental lines. Marker TG105 mapped 0.4 centiMorgan (CM) from I2. Physical analysis of TG105 and its flanking RFLP markers, TG26 and TG36, by pulsed field gradient gel electrophoresis (PFGE) yielded a restriction map for this region encompassing at least 620 kb of the tomato genome. TG105 and TG26 hybridized to the same 175 kb MluI-NruI restriction fragment. We have therefore linked two genetically distinct RFLP markers. Based on the 4.1 cM distance between them, we have assigned a mean value of 43 kb for each cM recombination distance in the vicinity of I2. This local ratio between physical and genetic distances is more than 10-fold below the average for the tomato genome. It should therefore be possible to clone I2 by chromosome walking from TG105.
显性基因I2赋予番茄(Lycopersicon esculentum)对尖孢镰刀菌番茄专化型2号生理小种的抗性。最近发现一个限制性片段长度多态性(RFLP)标记TG105与I2紧密连锁。通过反向遗传学方法克隆该基因的可能性促使我们从遗传和物理层面详细描述11号染色体上I2基因座周围的区域。我们分析了140株由抗镰刀菌和感病亲本杂交产生的F2植株中11号染色体上RFLP标记的分离模式以及对镰刀菌的抗性。标记TG105与I2的遗传距离为0.4厘摩(cM)。通过脉冲场梯度凝胶电泳(PFGE)对TG105及其侧翼RFLP标记TG26和TG36进行物理分析,得到了该区域的限制性图谱,该区域至少涵盖620 kb的番茄基因组。TG105和TG26与同一条175 kb 的MluI - NruI限制性片段杂交。因此我们将两个遗传上不同的RFLP标记连接起来了。基于它们之间4.1 cM 的距离,我们得出在I2附近每个cM重组距离对应的平均物理距离值为43 kb。I2附近物理距离与遗传距离的这个局部比率比番茄基因组平均水平低10倍以上。因此应该可以从TG105开始通过染色体步移法克隆I2。