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苔藓植物小立碗藓的序列锚定遗传连锁图谱。

A sequence-anchored genetic linkage map for the moss, Physcomitrella patens.

作者信息

Kamisugi Yasuko, von Stackelberg Mark, Lang Daniel, Care Matthew, Reski Ralf, Rensing Stefan A, Cuming Andrew C

机构信息

Centre for Plant Sciences, Faculty of Biological Sciences, Leeds University, Leeds LS29JT, UK.

出版信息

Plant J. 2008 Dec;56(5):855-66. doi: 10.1111/j.1365-313X.2008.03637.x. Epub 2008 Jul 23.

Abstract

The moss Physcomitrella patens is a model for the study of plant cell biology and, by virtue of its basal position in land plant phylogeny, for comparative analysis of the evolution of plant gene function and development. It is ideally suited for 'reverse genetic' analysis by virtue of its outstanding ability to undertake targeted transgene integration by homologous recombination. However, gene identification through mutagenesis and map-based cloning has hitherto not been possible, due to the lack of a genetic linkage map. Using molecular markers [amplified fragment length polymorphisms (AFLP) and simple sequence repeats (SSR)] we have generated genetic linkage maps for Physcomitrella. One hundred and seventy-nine gene-specific SSR markers were mapped in 46 linkage groups, and 1574 polymorphic AFLP markers were identified. Integrating the SSR- and AFLP-based maps generated 31 linkage groups comprising 1420 markers. Anchorage of the integrated linkage map with gene-specific SSR markers coupled with computational prediction of AFLP loci has enabled its correspondence with the newly sequenced Physcomitrella genome. The generation of a linkage map densely populated with molecular markers and anchored to the genome sequence now provides a resource for forward genetic interrogation of the organism and for the development of a pipeline for the map-based cloning of Physcomitrella genes. This will radically enhance the potential of Physcomitrella for determining how gene function has evolved for the acquisition of complex developmental strategies within the plant kingdom.

摘要

小立碗藓(Physcomitrella patens)是研究植物细胞生物学的模式植物,由于其在陆地植物系统发育中的基础地位,也是用于比较分析植物基因功能和发育进化的模式植物。因其具有通过同源重组进行靶向转基因整合的卓越能力,它非常适合进行“反向遗传学”分析。然而,由于缺乏遗传连锁图谱,通过诱变和基于图谱的克隆来鉴定基因至今仍无法实现。我们利用分子标记[扩增片段长度多态性(AFLP)和简单序列重复(SSR)]构建了小立碗藓的遗传连锁图谱。179个基因特异性SSR标记被定位到46个连锁群中,同时鉴定出1574个多态性AFLP标记。整合基于SSR和AFLP的图谱,得到了由1420个标记组成的31个连锁群。通过基因特异性SSR标记对整合后的连锁图谱进行锚定,并结合AFLP位点的计算预测,使其与新测序的小立碗藓基因组相对应。现在,一个密集分布着分子标记并锚定到基因组序列的连锁图谱的构建,为对该生物体进行正向遗传学研究以及开发小立碗藓基因基于图谱克隆的流程提供了资源。这将极大地提升小立碗藓在确定基因功能如何进化以获取植物王国复杂发育策略方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a416/2667646/6304662296ce/tpj0056-0855-f1.jpg

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