Suppr超能文献

水稻半矮秆基因 sd-1。I. 与酯酶位点 Estl-2 的连锁。

The semidwarf gene, sd-1, of rice (Oryza sativa L.). I. Linkage with the esterase locus, Estl-2.

机构信息

Genetics Division, Agricultural Biotechnology Institute, RDA, 441-707, Suweon, Republic of Korea.

出版信息

Theor Appl Genet. 1994 Sep;89(1):49-53. doi: 10.1007/BF00226981.

Abstract

The linkage relationship between the semidwarf gene (sd-1) and the isozyme locus EstI-2 was elucidated using segregating populations derived from crosses between several semidwarf testers and tall rice varieties. Bimodal distributions for culm length were observed in F2 populations of three cross combinations, including Shiokari/Shiokari (sd-1), Taichung 65 (A,Pn,Pau)/Taichung 65 (sd-1), and Milyang 23/Kasalath. Taking the valley of the distribution curves as the dividing point, two height classes were apparent with a segregation ratio of 3 tall∶1 short, demonstrating this character to be under the control of a single recessive gene. An inheritance study of esterase isozymes, based on isoelectric focusing (IEF), showed that the EstI-2 locus had two active allozymes of monomeric structure and one null form, which were designated "a", "b", and "n", respectively (Eun et al. 1990). Semidwarf testers such as Shiokari (sd-1), Taichung 65 (sd-1) and Milyang 23 have 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 dividing F2 populations based on EstI-2 allozyme patterns, culmlength distributions exhibited trimodal curves. Most of the short plants had the 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. Einkage analysis indicated that sd-1 and EstI-2 were tightly linked. These findings were also confirmed by segregation analyses in F3 progenies. No recombinants among 171 F3 families from the Shiokari/Shiokari (sd-1) combination, five recombinants among 267 F3 families from Taichung 65 (A,Pn,Pau)/Taichung 65(sd-1), and only two recombinants out of 237 F3 families from Milyang 23/Kasalath, were found. The recombination values were 0, 1.87 and 0.8%, respectively.

摘要

使用来自几个半矮秆测试品种与高秆水稻品种杂交的分离群体,阐明了半矮秆基因(sd-1)与同工酶座位 EstI-2 之间的连锁关系。在三个杂交组合的 F2 群体中观察到了株高的双峰分布,包括 Shiokari/Shiokari(sd-1)、Taichung 65(A,Pn,Pau)/Taichung 65(sd-1)和 Milyang 23/Kasalath。以分布曲线的谷值为分界点,有两个高度类别,分离比为 3 个高∶1 个矮,表明该性状受单个隐性基因控制。基于等电聚焦(IEF)的酯酶同工酶遗传研究表明,EstI-2 座位有两个单体结构的活性等位基因和一个无效形式,分别命名为“a”、“b”和“n”(Eun 等人,1990 年)。Shiokari(sd-1)、Taichung 65(sd-1)和 Milyang 23 等半矮秆测试品种具有活性等位基因 EstI-2(aa),而高秆亲本 Shiokari 和 Taichung 65(A,Pn,Pau)具有活性等位基因 EstI-2(bb),而 Kasalath 具有该等位基因的无效形式 EstI-2(nn)。根据 EstI-2 等位酶模式将 F2 群体进行划分,株高分布呈现出三峰曲线。大多数矮秆植物具有短亲本的纯合 EstI-2(aa)模式,大多数高秆植物具有纯合模式 EstI-2(bb)或 EstI-2(nn),大多数中间植物具有杂合 EstI-2(ab)或 EstI-2(an)带型。连锁分析表明 sd-1 和 EstI-2 紧密连锁。这些发现也通过 Shiokari/Shiokari(sd-1)组合的 F3 后代的分离分析得到了证实。在 Shiokari/Shiokari(sd-1)组合的 171 个 F3 家系中没有发现重组,在 Taichung 65(A,Pn,Pau)/Taichung 65(sd-1)组合的 267 个 F3 家系中发现了 5 个重组,在 Milyang 23/Kasalath 组合的 237 个 F3 家系中仅发现了 2 个重组。重组值分别为 0、1.87 和 0.8%。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验