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七个参与真菌和细菌共生期间根转录重编程所需的百脉根基因。

Seven Lotus japonicus genes required for transcriptional reprogramming of the root during fungal and bacterial symbiosis.

作者信息

Kistner Catherine, Winzer Thilo, Pitzschke Andrea, Mulder Lonneke, Sato Shusei, Kaneko Takakazu, Tabata Satoshi, Sandal Niels, Stougaard Jens, Webb K Judith, Szczyglowski Krzysztof, Parniske Martin

机构信息

Sainsbury Laboratory, Norwich NR4 7UH, United Kingdom.

出版信息

Plant Cell. 2005 Aug;17(8):2217-29. doi: 10.1105/tpc.105.032714. Epub 2005 Jun 24.

DOI:10.1105/tpc.105.032714
PMID:15980262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182484/
Abstract

A combined genetic and transcriptome analysis was performed to study the molecular basis of the arbuscular mycorrhiza (AM) symbiosis. By testing the AM phenotype of nodulation-impaired mutants and complementation analysis, we defined seven Lotus japonicus common symbiosis genes (SYMRK, CASTOR, POLLUX, SYM3, SYM6, SYM15, and SYM24) that are required for both fungal and bacterial entry into root epidermal or cortical cells. To describe the phenotype of these mutants at the molecular level, we screened for differentiating transcriptional responses of mutant and wild-type roots by large-scale gene expression profiling using cDNA-amplified fragment length polymorphism. Two percent of root transcripts was found to increase in abundance during AM development, from which a set of AM-regulated marker genes was established. A Ser-protease (SbtS) and a Cys-protease (CysS) were also activated during root nodule development. AM-induced transcriptional activation was abolished in roots carrying mutations in common symbiosis genes, suggesting a central position of these genes in a pathway leading to the transcriptional activation of downstream genes. By contrast, AM fungus-induced gene repression appeared to be unaffected in mutant backgrounds, which indicates the presence of additional independent signaling pathways.

摘要

进行了一项联合基因和转录组分析,以研究丛枝菌根(AM)共生的分子基础。通过测试结瘤受损突变体的AM表型并进行互补分析,我们确定了七个日本百脉根常见共生基因(SYMRK、CASTOR、POLLUX、SYM3、SYM6、SYM15和SYM24),这些基因是真菌和细菌进入根表皮或皮层细胞所必需的。为了在分子水平上描述这些突变体的表型,我们使用cDNA扩增片段长度多态性通过大规模基因表达谱筛选突变体和野生型根的差异转录反应。发现在AM发育过程中有2%的根转录本丰度增加,据此建立了一组AM调控的标记基因。一种丝氨酸蛋白酶(SbtS)和一种半胱氨酸蛋白酶(CysS)在根瘤发育过程中也被激活。在常见共生基因发生突变的根中,AM诱导的转录激活被消除,这表明这些基因在导致下游基因转录激活的途径中处于中心位置。相比之下,AM真菌诱导的基因抑制在突变背景中似乎不受影响,这表明存在其他独立的信号通路。

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