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本文引用的文献

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Somaclonal variation - a novel source of variability from cell cultures for plant improvement.体细胞无性系变异——植物改良细胞培养的一种新的变异来源。
Theor Appl Genet. 1981 Oct;60(4):197-214. doi: 10.1007/BF02342540.
2
Linkage mapping of sbm-1, a gene conferring resistance to pea seed-borne mosaic virus, using molecular markers in Pisum sativum.利用豌豆中的分子标记对豌豆种传花叶病毒抗性基因 sbm-1 进行连锁作图。
Theor Appl Genet. 1993 Jan;85(5):609-15. doi: 10.1007/BF00220920.
3
Identification of RAPD markers linked to a gene governing cadmium uptake in durum wheat.鉴定与控制硬质小麦镉吸收有关基因连锁的 RAPD 标记。
Genome. 1995 Jun;38(3):543-7. doi: 10.1139/g95-070.
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Genome flux in tomato cell clones cultured in vitro in different physiological equilibria. II. A RAPD analysis of variability.番茄细胞克隆在不同生理平衡条件下离体培养的基因组流。II. 变异性的 RAPD 分析。
Genome. 1996 Oct;39(5):846-53. doi: 10.1139/g96-107.
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Development and characterization of SCAR markers linked to the citrus tristeza virus resistance gene from Poncirus trifoliata.开发和鉴定与枳属抗柑橘衰退病毒基因连锁的 SCAR 标记。
Genome. 1997 Oct;40(5):697-704. doi: 10.1139/g97-792.
6
Molecular mapping of a thermosensitive genetic male sterility gene in rice using bulked segregant analysis.利用分离群体分组分析法对水稻温敏雄性不育基因进行分子作图。
Genome. 1997 Apr;40(2):188-94. doi: 10.1139/g97-027.
7
[Identification and mapping of polymorphic RAPD markers of pea (Pisum sativum L.) genome].[豌豆(Pisum sativum L.)基因组多态性RAPD标记的鉴定与图谱构建]
Genetika. 2005 Mar;41(3):341-8.
8
[RAPD and ISSR analyses of regenerated pea Pisum sativum L. plants].[再生豌豆(Pisum sativum L.)植株的随机扩增多态性DNA(RAPD)和简单序列重复区间(ISSR)分析]
Genetika. 2005 Jan;41(1):71-7.
9
[Identification and mapping of chi115 gene and DNA markers linked to it in pea (Pisum sativum L.)].[豌豆(Pisum sativum L.)中chi115基因及其连锁DNA标记的鉴定与定位]
Genetika. 2004 Jul;40(7):909-15.
10
[Analysis of specific RAPD- and ISSR-fragments in somaclonal maize (Zea mays L.) and development of SCAR markers based on them].[体细胞克隆玉米(Zea mays L.)中特异性RAPD和ISSR片段分析及基于这些片段的SCAR标记开发]
Genetika. 2003 Dec;39(12):1664-72.

利用分子标记研究植物基因组变异。

Studying plant genome variation using molecular markers.

作者信息

Gostimsky S A, Kokaeva Z G, Konovalov F A

机构信息

Department of Genetics, Biological Faculty, Moscow State University, Moscow, 119899 Russia.

出版信息

Russ J Genet. 2005;41(4):378-388. doi: 10.1007/s11177-005-0101-1.

DOI:10.1007/s11177-005-0101-1
PMID:32214754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7088922/
Abstract

The authors' studies on the organization and variation of plant genome with the use of molecular markers are briefly reviewed with special emphasis on random amplified polymorphic DNA (RAPD), inter simple sequence repeat (ISSR), sequence characterized amplified region (SCAR), and cleaved amplified polymorphic sequence (CAPS) markers detected with the use of polymerase chain reaction (PCR). These markers have been demonstrated to be promising for identifying cultivars and determining the purity of genetic strains of pea. Genetic relationships between strains, cultivars, and mutants of pea have been studied. The role of molecular markers in molecular genetic mapping and localizing the genes of commercially important characters of pea has been shown. The possibility of the use of molecular markers for studying somaclonal variation and detecting mutagenic factors in plants during long-term spaceflights is considered. The prospects of using DNA markers for understanding the organization and variability of higher plant genomes are discussed.

摘要

简要回顾了作者利用分子标记对植物基因组的组织和变异进行的研究,特别强调了利用聚合酶链反应(PCR)检测的随机扩增多态性DNA(RAPD)、简单序列重复区间(ISSR)、序列特异性扩增区域(SCAR)和酶切扩增多态性序列(CAPS)标记。这些标记已被证明在鉴定豌豆品种和确定遗传菌株纯度方面很有前景。研究了豌豆菌株、品种和突变体之间的遗传关系。展示了分子标记在分子遗传图谱绘制以及定位豌豆重要商业性状基因方面的作用。考虑了利用分子标记研究体细胞克隆变异以及检测植物在长期太空飞行过程中诱变因素的可能性。讨论了使用DNA标记理解高等植物基因组组织和变异性的前景。