International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, 110 067, New Delhi, India.
Theor Appl Genet. 1995 Nov;91(6-7):978-86. doi: 10.1007/BF00223909.
Forty-seven recombinant inbred (RI) lines derived from a cross between two indica rices, cv 'Phalguna' and the Assam land race ARC 6650, were subjected to restriction fragment length polymorphism (RFLP) analysis using cloned probes defining 150 single-copy loci uniformly dispersed on the 12 chromosomes of rice. Of the probes tested, 47 detected polymorphism between the parents. Heterozygosity was calculated for each line and for each of the polymorphic loci. Average heterozygosity per line was 9.6% but was excessive (>20%) in the 5 lines that seemed to have undergone outcrossing immediately prior to harvest. Average heterozygosity detected by each probe across the 47 RI lines was 9.7%. The majority of probes revealed the low level of heterozygosity (<8%) expected for F5-F6 lines in a species showing about 5% outbreeding. On the other hand, 7 probes exhibited heterozygosity in excess of 15%, while with a eighth probe (RG2 from chromosome 11) heterozygosity varied according to the restriction enzyme employed, ranging from 2% with SaII to 72% with EcoRV. The presence of 34 recombination sites in a segment of the genome as short as 24 kb indicates a strong selection for recombination between two neighbouring loci, one required as homozygous for the 'Phalguna' allele, and the other heterozygous. Since selection was principally for yield advantage over that of the high-yielding parent, 'Phalguna', one or both of these loci may be important for heterosis in this cross. The results also indicate that heterozygosity as measured by RFLP can depend on the particular restriction endonuclease employed.
四十七株重组近交系(RI)是由籼稻品种“Phalguna”和 Assam 地方品种 ARC 6650 杂交衍生而来,用克隆探针进行了限制片段长度多态性(RFLP)分析,这些探针定义了 150 个单拷贝基因座,均匀分布在水稻的 12 条染色体上。在所测试的探针中,有 47 个探针在亲本间检测到多态性。每个系和每个多态性基因座都计算了杂合性。每个系的平均杂合度为 9.6%,但在 5 个似乎在收获前经历了异交的系中,杂合度过高(>20%)。47 个 RI 系中每个探针检测到的平均杂合度为 9.7%。大多数探针显示出在一个种内表现出约 5%的杂交率的情况下,F5-F6 系中预期的低水平杂合度(<8%)。另一方面,有 7 个探针表现出超过 15%的杂合度,而第八个探针(来自 11 号染色体的 RG2)的杂合度因所用的限制酶而异,SaII 的杂合度为 2%,EcoRV 的杂合度为 72%。在短短 24kb 的基因组片段中存在 34 个重组位点表明,两个相邻基因座之间存在强烈的重组选择,一个基因座需要为“Phalguna”等位基因纯合,另一个基因座杂合。由于选择主要是为了获得比高产亲本“Phalguna”更高的产量优势,因此这两个基因座中的一个或两个可能对该杂交种的杂种优势很重要。结果还表明,通过 RFLP 测量的杂合度可能取决于所使用的特定限制内切酶。