THE SEMIDWARF GENE, SD-1, OF RICE (ORYZA-SATIVA L) .1. LINKAGE WITH THE ESTERASE LOCUS, ESTI-2

Citation
Yg. Cho et al., THE SEMIDWARF GENE, SD-1, OF RICE (ORYZA-SATIVA L) .1. LINKAGE WITH THE ESTERASE LOCUS, ESTI-2, Theoretical and Applied Genetics, 89(1), 1994, pp. 49-53
Citations number
25
Categorie Soggetti
Genetics & Heredity
ISSN journal
00405752
Volume
89
Issue
1
Year of publication
1994
Pages
49 - 53
Database
ISI
SICI code
0040-5752(1994)89:1<49:TSGSOR>2.0.ZU;2-1
Abstract
The linkage relationship between the semidwarf gene (sd-1) and the iso zyme locus EstI-2 was elucidated using segregating populations derived from crosses between several semidwarf testers and tall rice varietie s. Bimodal distributions for culm length were observed in F-2 populati ons of three cross combinations, including Shiokari/Shiokari (sd-1), T aichung 65 (A, Pn, Pau)/Taichung 65 (sd-1), and Milyang 23/Kasalath. T aking the valley of the distribution curves as the dividing point, two height classes were apparent with a segregation ratio of 3 tall:1 sho rt, demonstrating this character to be under the control of a single r ecessive gene. An inheritance study of esterase isozymes, based on iso electric focusing (IEF), showed that the EstI-2 locus had two active a llozymes of monomeric structure and one null form, which were designat ed ''a'', ''b'', and ''n'', respectively (Eun et al. 1990). Semidwarf testers such as Shiokari (sd-1), Taichung 65 (sd-1) and Milyang 23 hav e an active allozyme designated as EstI-2(aa), while the tall parents, Shiokari and Taichung 65 (A,Pn,Pau), have the active allozyme, EstI-2 (bb) and Kasalath has a null form of the allozyme, EstI-2(nn). By divi ding F-2 populations based on EstI-2 allozyme patterns, culm-length di stributions exhibited trimodal curves. Most of the short plants had th e homozygous EstI-2(aa) pattern of the short parents, most of the tall plants had the homozygous pattern, EstI-2(bb) Or EstI-2(nn), and most of the intermediate plants had the heterozygous EstI-2(ab) or EstI-2( an) banding pattern. Linkage analysis indicated that sd-1 and EstI-2 w ere tightly linked. These findings were also confirmed by segregation analyses in F-3 progenies. No recombinants among 171 F-3 families from the Shiokari/Shiokari (sd-1) combination, five recombinants among 267 F-3 families from Taichung 65 (A, Pn, Pau)/Taichung 65(sd-1), and onl y two recombinants out of 237 F-3 families from Milyang 23/Kasalath, w ere found. The recombination values were 0, 1.87 and 0.8%, respectivel y.