期刊文献+

目标起始密码子多态性(SCoT):一种基于翻译起始位点的目的基因标记新技术 被引量:91

SCoT:A Novel Gene Targeted Marker Technique Based on the Translation Start Codon
下载PDF
导出
摘要 随着功能基因组学的发展,分子标记领域已开始从传统的随机或匿名性分子标记转向目的基因标记和功能性标记。目标起始密码子多态性(start codon targeted polymorphism,SCoT)标记是一种基于翻译起始位点的目的基因标记新技术,具有操作简单、重复性好等特点,根据ATG翻译起始位点侧翼保守序列来设计单引物,扩增产生偏向候选功能基因区显性多态性标记,适合不同层次实验室的不同领域的广泛应用,SCoT标记已开始在水稻和花生上得到运用。本文旨在介绍给研究者一种可以作为传统的RAPD、ISSR标记有效补充的目的基因标记新技术,希望其广泛的应用于生物多样性分析、遗传图谱构建、重要性状标记等方面。 With the development of functional genomics, the area of molecular markers has witnessed a shift from the so-called random DNA markers (RDMs) or anonymous markers to gene-targeted markers (GTMs) and functional markers (FMs). Start codon targeted polymorphism (SCOT) is a novel gene targeted marker technique based on the translation start codon with the characteristics of simplicity and reproducibility. The primers for SCoT marker analysis were designed based on the short conserved region surrounding the ATG translation start (or initiation) codon. Conducting PCR amplification using the designed single primer can generate dominant polymorphic markers with a bias toward candidate functional genes region. The SCoT technique can be widely applied to different fields in different laboratories. SCoT polymorphism marker technique has been successfully applied in rice and peanut. The objectives of this article are to introduce a novel gene targeted molecular marker technique complementary to conventional RAPD, ISSR to researchers and to wish it to be widely exploited in the fields of genetic diversity, genetic map constructing and important agronomic traits tagging.
出处 《分子植物育种》 CAS CSCD 2009年第3期635-638,共4页 Molecular Plant Breeding
基金 国家自然科学基金项目(30660094) 国家863计划(AA10A104) 广西科学基金项目(桂科自0832088) 广西科技攻关项目(桂科攻0815008-1-4)共同资助
关键词 SCoT标记技术 基因目的标记 功能性标记 单引物扩增反应 SCoT marker technique, Gene targeted marker (GTM), Functional marker (FM), Single primer amplification reaction (SPAR)
  • 相关文献

参考文献23

  • 1Andersen J.R., and Lobberstedt T., 2003, Functional markers in plants, Trends Plant Sci., 8(11): 554-560
  • 2Collard B.C.Y., and Mackill D.J., 2009, Start codon targeted (SCOT) polymorphism: a simple, novel DNA marker technique for generating gene-targeted markers in plants, Plant Mol. Biol. Rep., 27(1): 86-93
  • 3Fulton T.M., van der Hoeven R., Eannetta N.T., and Tanksley S.D., 2002, Identification, analysis, and utilization of conserved ortholog set markers for comparative genomics in higher plants, Plant Cell, 14(7): 1457-1467
  • 4Gupta P.K., and Rustgi S., 2004, Molecular markers from the transcribed/expressed region of the genome in higher plants, Funct. !ntegr. Genomics, 4(3): 139-162
  • 5Gupta M., Chyi Y.S., Romero-Severson J., and Owen J.L., 1994, Amplification of DNA markers from evolutionarily diverse genomes using single primers of SSRs, Theor. Appl. Genet., 89(7-8): 998-1006
  • 6Hawkins J.D., 1998, A survey on intron and exon lengths, Nucleic Acids Res., 16(21): 9893-9905
  • 7Hayes A.J., and Saghai Maroof M.A., 2000, Targeted resistance gene mapping in soybean using modified AFLPs, Theor. Appl. Genet., 100(8): 1279-1283
  • 8Hu J.G., and Vick B.A., 2003, Target region amplification polymorphism: a novel marker technique for plant genotyping, Plant Mol. Bio. Rep., 21(3): 289-294
  • 9Joshi C.P., Zhou H., Huang X., and Chiang V.L., 1997, Context sequences of translation initiation codon in plants, Plant Mol. Biol., 35(6): 993-1001
  • 10Li G.., and Quiros C.F., 2001, Sequence-related amplified poly-morphism (SRAP), a new marker system based on a simple PCR reaction: its application to mapping and gene tagging in Brassica, Theor. Appl. Genet., 103(2-3): 455-461

二级参考文献90

  • 1Wang-Zhen Guo Guo-Jia Ma Yi-Chao Zhu Chen-Xin Yi Tian-Zhen Zhang.Molecular Tagging and Mapping of Quantitative Trait Loci for Lint Percentage and Morphological Marker Genes in Upland Cotton[J].Journal of Integrative Plant Biology,2006,48(3):320-326. 被引量:14
  • 2Sturtevant A H. The linear arrangement of six sex-linked factors in Drosophila, as shown by their mode of association. Journal of Experimental Zoology, 1913, 14: 43-59.
  • 3Sax K. The association of size differences with seed-coat pattern and pigmentation in Phaseolus vulgaris. Genetics, 1923, 8: 552-560.
  • 4Henry R J. Plant Genotyping. CABI Publishing, 2001.
  • 5Grodzicker T, Anderson C, Sharp P A, Sambrook J. Conditional lethal mutants of adenovirus 2-simian virus 40 hybrids. I. Host range mutants of Ad2+ND1. The Journal of Virology, 1974, 13(6): 1237-1244.
  • 6Williams J G K, Kubelik A R, Livak K J, Rafalski J A, Tingey S V. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers Nucleic Acid Research, 1990, 18:6531-6535.
  • 7Cardle I, Ramsay L, Milboume D, Macaulay M, Marshall D, Waugh R. Computation and experimental characterization of physically clustered simple sequence repeats in plants. Genetices, 2000, 156: 847-854.
  • 8Powell W, Morgante M, Andre C, Hanafey M, Vogel J, Tingey S, Rafalski A. The comparison of RFLP, RAPDs, AFLP and SSR (microsatellite) markers for germplasm analysis. Molecular Breeding, 1996, 2: 225-238.
  • 9Wang D G, Fan J B, Siao C J, Bemo A, Young P, Sapolsky R, Ghandour G, Perkins N, Winchester E, Spencer J. Large-scale identification mapping and genotyping of single nuclotide polymorphisms in the human genome. Science, 1998: 280:1077-1082.
  • 10Gupta P K, Varshney R K, Prasad M. Molecular markers: principles and methodology. In: Jain S M. Molecular Techniques in Crop Improvement. Kluwer Academic Publishers, 2002: 9-54.

共引文献77

同被引文献1189

引证文献91

二级引证文献509

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部