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利用cDNA筛选技术在整合的高粱遗传图谱和物理图谱上定位基因。

Mapping genes on an integrated sorghum genetic and physical map using cDNA selection technology.

作者信息

Childs K L, Klein R R, Klein P E, Morishige D T, Mullet J E

机构信息

Institute for Plant Genomics and Biotechnology, Texas A&M University, College Station, TX 77843, USA.

出版信息

Plant J. 2001 Aug;27(3):243-55. doi: 10.1046/j.1365-313x.2001.01085.x.

Abstract

Sorghum is an important target of plant genomics. This cereal has unusual tolerance to adverse environments, a small genome (750 Mbp) relative to most other grasses, a diverse germplasm, and utility for comparative genomics with rice, maize and other grasses. In this study, a modified cDNA selection protocol was developed to aid the discovery and mapping of genes across an integrated genetic and physical map of the sorghum genome. BAC DNA from the sorghum genome map was isolated and covalently bound in arrayed tubes for efficient liquid handling. Amplifiable cDNA sequence tags were isolated by hybridization to individual sorghum BACs, cloned and sequenced. Analysis of a fully sequenced sorghum BAC indicated that about 80% of known or predicted genes were detected in the sequence tags, including multiple tags from different regions of individual genes. Data from cDNA selection using the fully sequenced BAC indicate that the occurrence of mislocated cDNA tags is very low. Analysis of 35 BACs (5.25 Mb) from sorghum linkage group B revealed (and therefore mapped) two sorghum genes and 58 sorghum ESTs. Additionally, 31 cDNA tags that had significant homologies to genes from other species were also isolated. The modified cDNA selection procedure described here will be useful for genome-wide gene discovery and EST mapping in sorghum, and for comparative genomics of sorghum, rice, maize and other grasses.

摘要

高粱是植物基因组学的重要研究对象。这种谷物对恶劣环境具有非同寻常的耐受性,相对于大多数其他禾本科植物而言,其基因组较小(750兆碱基对),种质资源多样,并且在与水稻、玉米及其他禾本科植物进行比较基因组学研究方面具有实用价值。在本研究中,开发了一种改良的cDNA筛选方案,以助力在高粱基因组的整合遗传图谱和物理图谱上发现基因并进行基因定位。从高粱基因组图谱中分离出BAC DNA,并将其共价结合在排列好的试管中,以便进行高效的液体处理。通过与单个高粱BAC杂交分离出可扩增的cDNA序列标签,进行克隆和测序。对一个已完全测序的高粱BAC的分析表明,在序列标签中检测到了约80%的已知或预测基因,包括来自单个基因不同区域的多个标签。使用已完全测序的BAC进行cDNA筛选的数据表明,错定位的cDNA标签的出现率非常低。对高粱连锁群B中的35个BAC(5.25兆碱基对)进行分析,发现(并因此定位了)两个高粱基因和58个高粱EST。此外,还分离出了31个与其他物种的基因具有显著同源性的cDNA标签。本文所述的改良cDNA筛选程序将有助于高粱全基因组的基因发现和EST定位,以及高粱、水稻、玉米和其他禾本科植物的比较基因组学研究。

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