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利用叶绿体单核苷酸多态性(SNP)标记对杨属物种进行鉴定——这对可理解和可靠的杨树育种至关重要。

Differentiation of Populus species using chloroplast single nucleotide polymorphism (SNP) markers--essential for comprehensible and reliable poplar breeding.

机构信息

Johann Heinrich von Thünen Institute, Institute for Forest Genetics, Grosshansdorf, Germany.

出版信息

Plant Biol (Stuttg). 2012 Mar;14(2):374-81. doi: 10.1111/j.1438-8677.2011.00502.x. Epub 2011 Aug 25.

DOI:10.1111/j.1438-8677.2011.00502.x
PMID:21973311
Abstract

Within the genus Populus several species belonging to different sections are cross-compatible. Hence, high numbers of interspecies hybrids occur naturally and, additionally, have been artificially produced in huge breeding programmes during the last 100 years. Therefore, determination of a single poplar species, used for the production of 'multi-species hybrids' is often difficult, and represents a great challenge for the use of molecular markers in species identification. Within this study, over 20 chloroplast regions, both intergenic spacers and coding regions, have been tested for their ability to differentiate different poplar species using 23 already published barcoding primer combinations and 17 newly designed primer combinations. About half of the published barcoding primers yielded amplification products, whereas the new primers designed on the basis of the total sequenced cpDNA genome of Populus trichocarpa Torr. & Gray yielded much higher amplification success. Intergenic spacers were found to be more variable than coding regions within the genus Populus. The highest discrimination power of Populus species was found in the combination of two intergenic spacers (trnG-psbK, psbK-psbl) and the coding region rpoC. In barcoding projects, the coding regions matK and rbcL are often recommended, but within the genus Populus they only show moderate variability and are not efficient in species discrimination.

摘要

在杨属内,有几个属于不同组的种是相互可杂交的。因此,大量的种间杂种自然发生,此外,在过去的 100 年中,在大规模的育种计划中也被人为地产生。因此,确定用于生产“多物种杂种”的单一杨树种通常是困难的,并且代表了在物种鉴定中使用分子标记的巨大挑战。在本研究中,已经使用 23 种已发表的条形码引物组合和 17 种新设计的引物组合,测试了超过 20 个叶绿体区域,包括基因间间隔区和编码区,以确定它们区分不同杨树种的能力。大约一半的已发表的条形码引物产生了扩增产物,而基于 Populus trichocarpa Torr. & Gray 的全序列 cpDNA 基因组设计的新引物则产生了更高的扩增成功率。在杨属内,基因间间隔区比编码区具有更高的变异性。在两个基因间间隔区(trnG-psbK,psbK-psbl)和编码区 rpoC 的组合中,发现对杨属物种的区分能力最高。在条形码项目中,经常推荐使用编码区 matK 和 rbcL,但在杨属内,它们的变异性仅为中等,并且在物种鉴别中效率不高。

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