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番茄遗传变异的同工酶监测

Isozyme monitoring of genetic variation in Lycopersicon.

作者信息

Rick C M, Tanksley S D

出版信息

Isozymes Curr Top Biol Med Res. 1983;11:269-84.

PMID:6642990
Abstract

Linkages with isozymic loci facilitate the investigation of certain classes of genetic variation. Due to the mapping of 20 isozymic loci on nine of the 12 chromosomes of the cultivated tomato (Lycopersicon esculentum), much progress has been made in these applications, particularly in the analysis of interspecific hybrids. Isozymes can expedite the selective elimination of inferior wild parent germ plasm in backcross transfer of desired genes to the cultivated parent. Allelic isozyme constitution also aids in identification of lines, particularly in evaluating the purity of F1 hybrid cultivars. Advantages that isozymes impart to such investigations are: (1) unequivocal classification of phenotypes, (2) detection of heterozygotes, (3) lack of epistasis between isozyme loci, (4) lack of effect of allelic isozymes per se on morphology or physiology, (5) prolific source of monogenic markers, and (6) phenotyping at early developmental stages. Each of these attributes can be exploited to great advantage, but collectively they constitute a formidable argument for monitoring genetic variation by means of isozymes. Linkages between isozyme loci and qualitative loci can be exploited as in the monitoring of Mi (gene for root-knot nematode resistance derived from L peruvianum) by the very tightly linked Aps-1(1); in similar fashion, Prx-2(1) serves as a useful marker for ms-10 (male sterility). Asp-1 monitoring in the former is more reliable than testing for nematode resistance per se; codominance of Prx-2 alleles of the latter solves problems incurred by the recessiveness of ms-10; in both instances phenotypes can be ascertained at earlier growth stages for isozymes than for economic traits. In the first backcross of the interspecific hybrid L esculentum x Solanum pennellii to the former, the segregation of four quantitative traits was monitored by allelic isozymes at 12 loci, situated on at least eight chromosomes, covering approximately 60% of the known tomato genome. At least five quantitative trait loci (QTL) were found to determine each of the four traits. Each parent contributes alleles with positive as well as negative effects, the greatest balance for stigma exsertion, the trait also exhibiting the greatest extent of transgressive segregation. Three pairs of linked isozymic loci permitted a crude form of three-point mapping of the associated QTL. interactions between QTL linked with pairs of isozymic genes were tested in all possible combinations; 18 of the 274 comparisons showed significant interactions, indicating epistasis.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

与同工酶基因座的连锁有助于对某些类型的遗传变异进行研究。由于已在栽培番茄(Lycopersicon esculentum)12条染色体中的9条上绘制了20个同工酶基因座的图谱,因此在这些应用方面已取得了很大进展,特别是在种间杂种分析方面。同工酶可以加快在将所需基因回交转移到栽培亲本的过程中对劣质野生亲本种质的选择性消除。等位基因同工酶组成也有助于品系鉴定,特别是在评估F1杂交品种的纯度方面。同工酶赋予此类研究的优势包括:(1)表型的明确分类;(2)杂合子的检测;(3)同工酶基因座之间不存在上位性;(4)等位基因同工酶本身对形态或生理没有影响;(5)丰富的单基因标记来源;(6)在发育早期进行表型分析。这些特性中的每一个都可以被充分利用,但总体而言,它们构成了通过同工酶监测遗传变异的有力论据。同工酶基因座与质量性状基因座之间的连锁可以像通过紧密连锁的Aps-1(1)监测Mi(源自秘鲁番茄的根结线虫抗性基因)那样被利用;以类似的方式,Prx-2(1)作为ms-10(雄性不育)的有用标记。在前者中对Asp-1的监测比直接检测线虫抗性更可靠;后者中Prx-2等位基因的共显性解决了ms-10隐性所带来的问题;在这两种情况下,对于同工酶而言,在生长早期就可以确定表型,而对于经济性状则不然。在种间杂种L esculentum x Solanum pennellii与前者的首次回交中,通过位于至少8条染色体上的12个基因座的等位基因同工酶监测了4个数量性状的分离,这些染色体覆盖了已知番茄基因组的约60%。发现至少5个数量性状基因座(QTL)决定了这4个性状中的每一个。每个亲本贡献的等位基因既有正向效应也有负向效应,对于柱头外露来说平衡最大,该性状也表现出最大程度的超亲分离。三对连锁的同工酶基因座允许对相关QTL进行粗略的三点定位。对与成对同工酶基因连锁的QTL之间的相互作用进行了所有可能组合的测试;274次比较中的18次显示出显著的相互作用,表明存在上位性。(摘要截选至400字)

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