Trisomic analysis of new gene for late heading in rice, Oryza sativa L

被引:5
|
作者
Khun, Leang Hak [1 ]
Miyaji, Shuhei
Motomura, Keiji
Murayama, Seiichi
Adaniya, Shinichi
Nose, Akihiro
机构
[1] Kagoshima Univ, United Grad Sch Agr Sci, Kagoshima 8900065, Japan
[2] Univ Rykyus, Fac Agr, Nishihara, Okinawa 9030213, Japan
[3] Saga Univ, Fac Agr, Saga 8408502, Japan
[4] Independent Adm Inspect, Kodaira, Tokyo 1870011, Japan
关键词
allelism test; heading time; lateness gene; rice; trisomic analysis;
D O I
10.1007/s10681-006-9145-0
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
A near isogenic line, T65-LH7 bred from a rice variety, Ketan Nangka by five times of successive backcrossing with Taichung 65 (T65) as recurrent parent was found to carry a recessive lateness gene tentatively designated as ef6(t). The present study was performed to investigate the allelic relationships between ef6(t) and other heading time genes, Ef1, Efx, ef2(t), ef3(t), ef4(t) and ef5 by allelism test and to locate the chromosomal location of ef6(t) by trisomic analysis. In allelism test, six testers carrying each of heading time genes, Ef1, Efx, ef2(t), ef3(t), ef4(t) and ef5 were used. Those testers were the near isogenic lines of T65. T65-LH7 was crossed with respective testers. Heading times in F-2 and/or B1F1 plants were examined. All F-2 and/or B1F1 populations derived from those crosses exhibited digenic segregations, respectively. These results suggested that ef6(t) was independent of Ef1, Efx, ef2(t), ef3(t), ef4(t) and ef5. Sub sequently, trisomic analysis of ef6(t) was performed using seven Triplo lines having extra chromosomes, 2, 4, 5, 7, 9, 10 and 12. These Triplo lines were the near isogenic lines of T65. They were used as maternal parent to cross with T65-LH7. Heading times in F-2 plants obtained from self-pollination of F-1 plants were observed. Among F-2 plants examined only those derived from a cross between Triplo-7 and T65-LH7 showed a typical trisomic segregation manner, suggesting that ef6(t) was located on chromosome 7. Consequently, the nomenclature of the present gene should be designated as ef6.
引用
收藏
页码:235 / 241
页数:7
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