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香脂冷杉(Calocedrus decurrens)中影响苹果酸脱氢酶同工酶电泳迁移率的一个基因座的鉴定及其在种群研究中的意义。

Identification of a locus modifying the electrophoretic mobility of malate dehydrogenase isozymes in incense-cedar (Calocedrus decurrens), and its implications for population studies.

作者信息

Harry D E

出版信息

Biochem Genet. 1983 Jun;21(5-6):417-34. doi: 10.1007/BF00484435.

DOI:10.1007/BF00484435
PMID:6870770
Abstract

Using megagametophyte (maternal haploid) and embryo (diploid) tissues of incense-cedar seeds, the expression of one of three malate dehydrogenase (MDH) loci was found to be influenced by a second, unlinked, modifier locus. Whereas alleles of the affected structural locus are codominant, the modifier alleles show dominance. The action of the modifier, limited to 1 of 28 structural loci examined, results in a shift of electrophoretic mobility detectable in conventional starch gels. Both the structural and the modifier MDH loci are polymorphic in all populations surveyed. Studies of genetic variation in natural populations made without rigorous genetic analysis may not detect such modification. By misinterpreting the genetic basis of enzyme phenotypes, such undetected modification can result in overestimates of genetic diversity in natural populations and can cause an apparent excess of homozygotes relative to expectations. These effects on allele and genotype frequency estimates are dependent on the levels of polymorphism at both the structural and the modifier loci. Using procedures common to many surveys of electrophoretic variation, the frequency of a recessive modifier allele could be as high as 0.3 before being detected.

摘要

利用香柏种子的雌配子体(母本单倍体)和胚(二倍体)组织,发现三个苹果酸脱氢酶(MDH)位点之一的表达受到另一个不连锁的修饰位点的影响。受影响的结构位点的等位基因是共显性的,而修饰位点的等位基因表现出显性。修饰作用仅限于所检测的28个结构位点中的1个,其结果是在传统淀粉凝胶中可检测到电泳迁移率的改变。结构和修饰MDH位点在所有被调查的群体中都是多态的。在没有进行严格遗传分析的情况下对自然群体的遗传变异进行研究,可能检测不到这种修饰。由于错误解读酶表型的遗传基础,这种未被检测到的修饰可能导致对自然群体遗传多样性的高估,并可能导致相对于预期而言纯合子明显过多。这些对等位基因和基因型频率估计的影响取决于结构位点和修饰位点的多态水平。使用许多电泳变异调查中常见的方法,一个隐性修饰等位基因在被检测到之前的频率可能高达0.3。

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Identification of a locus modifying the electrophoretic mobility of malate dehydrogenase isozymes in incense-cedar (Calocedrus decurrens), and its implications for population studies.香脂冷杉(Calocedrus decurrens)中影响苹果酸脱氢酶同工酶电泳迁移率的一个基因座的鉴定及其在种群研究中的意义。
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本文引用的文献

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Genetic control of multiple esterases from needles and macrogametophytes ofPicea abies.遗传控制来自云杉针和大配子体的多种酯酶。
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A gene modifying mitochondrial malate dehydrogenase isozymes in Sorghum (Gramineae).一种修饰高粱(禾本科)线粒体苹果酸脱氢酶同工酶的基因。
Biochem Genet. 1986 Dec;24(11-12):813-9. doi: 10.1007/BF00554521.
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Genetic control of acid phosphatase Rm and its relation to control of peroxidase Rm in flax (Linum) genotrophs.亚麻(亚麻属)基因型中酸性磷酸酶Rm的遗传控制及其与过氧化物酶Rm控制的关系。
Biochem Genet. 1986 Jun;24(5-6):369-83. doi: 10.1007/BF00499093.
6
Relative mobility and activity of leaf malate dehydrogenase in flax (Linum usitatissimum) genotrophs and genotypes.亚麻(Linum usitatissimum)营养型和基因型中叶苹果酸脱氢酶的相对迁移率和活性
Biochem Genet. 1988 Apr;26(3-4):261-75. doi: 10.1007/BF00561465.
7
Malate dehydrogenase isozymes in flax genotroph leaves: differences in apparent molecular weight and charge between and within L and S.亚麻营养缺陷型叶片中的苹果酸脱氢酶同工酶:L型和S型之间以及L型和S型内部表观分子量和电荷的差异
Biochem Genet. 1988 Apr;26(3-4):249-60. doi: 10.1007/BF00561464.
Theor Appl Genet. 1978 Jul;52(4):145-57. doi: 10.1007/BF00282571.
4
Genetic control of malate dehydrogenase isozymes in maize.玉米中苹果酸脱氢酶同工酶的遗传控制。
Genetics. 1980 Jan;94(1):153-68. doi: 10.1093/genetics/94.1.153.
5
Structural VS. Post-Translational Components of Genic Variation-a Reply.基因变异的结构与翻译后成分——回应
Genetics. 1979 Jun;92(2):683-4. doi: 10.1093/genetics/92.2.683.
6
Structural VS. Post-Translational Component of Genic Variation.基因变异的结构成分与翻译后成分
Genetics. 1979 Jun;92(2):679-82. doi: 10.1093/genetics/92.2.679.
7
The Genetics of Electrophoretic Variation-a Reply.电泳变异的遗传学——一篇回应
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9
A pseudoduplication in Lycopersicon pimpinellifolium.醋栗番茄中的假重复。
Proc Natl Acad Sci U S A. 1979 Jul;76(7):3435-9. doi: 10.1073/pnas.76.7.3435.
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Microgeographical Variation in Allozyme Frequencies in Avena barbata.野燕麦等位酶频率的微观地理变异
Proc Natl Acad Sci U S A. 1972 Aug;69(8):2100-4. doi: 10.1073/pnas.69.8.2100.