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蒺藜苜蓿根瘤表达序列标签分析

Analysis of Medicago truncatula nodule expressed sequence tags.

作者信息

Györgyey J, Vaubert D, Jiménez-Zurdo J I, Charon C, Troussard L, Kondorosi A, Kondorosi E

机构信息

Institut des Sciences Végétales, CNRS, Gif-sur-Yvette, France.

出版信息

Mol Plant Microbe Interact. 2000 Jan;13(1):62-71. doi: 10.1094/MPMI.2000.13.1.62.

Abstract

Systematic sequencing of expressed sequence tags (ESTs) can give a global picture of the assembly of genes involved in the development and function of organs. Indeterminate nodules representing different stages of the developmental program are especially suited to the study of organogenesis. With the vector lambdaHybriZAP, a cDNA library was constructed from emerging nodules of Medicago truncatula induced by Sinorhizobium meliloti. The 5' ends of 389 cDNA clones were sequenced, then these ESTs were analyzed both by sequence homology search and by studying their expression in roots and nodules. Two hundred fifty-six ESTs exhibited significant similarities to characterized data base entries and 40 of them represented 26 nodulin genes, while 133 had no similarity to sequences with known function. Only 60 out of the 389 cDNA clones corresponded to previously submitted M. truncatula EST sequences. For 117 cDNAs, reverse Northern (RNA) hybridization with root and nodule RNA probes revealed enhanced expression in the nodule, 48 clones are likely to code for novel nodulins, 33 cDNAs are clones of already known nodulin genes, and 36 clones exhibit similarity to other characterized genes. Thus, systematic analysis of the EST sequences and their expression patterns is a powerful way to identify nodule-specific and nodulation-related genes.

摘要

对表达序列标签(ESTs)进行系统测序,可以全面了解参与器官发育和功能的基因组合情况。代表发育程序不同阶段的不定根瘤特别适合用于器官发生的研究。利用λHybriZAP载体,构建了由苜蓿中华根瘤菌诱导的蒺藜苜蓿新出现根瘤的cDNA文库。对389个cDNA克隆的5′端进行了测序,然后通过序列同源性搜索以及研究它们在根和根瘤中的表达对这些ESTs进行了分析。256个ESTs与已鉴定的数据库条目表现出显著相似性,其中40个代表26个根瘤蛋白基因,而133个与已知功能的序列没有相似性。389个cDNA克隆中只有60个与先前提交的蒺藜苜蓿EST序列相对应。对于117个cDNA,用根和根瘤RNA探针进行的反向Northern(RNA)杂交显示在根瘤中表达增强,48个克隆可能编码新的根瘤蛋白,33个cDNA是已知根瘤蛋白基因的克隆,36个克隆与其他已鉴定基因表现出相似性。因此,对EST序列及其表达模式进行系统分析是鉴定根瘤特异性和根瘤形成相关基因的有力方法。

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