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首页> 外文期刊>Plant Molecular Biology >A novel gene whose expression in Medicago truncatula roots is suppressed in response to colonization by vesicular-arbuscular mycorrhizal (VAM) fungi and to phosphate nutrition.
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A novel gene whose expression in Medicago truncatula roots is suppressed in response to colonization by vesicular-arbuscular mycorrhizal (VAM) fungi and to phosphate nutrition.

机译:一个新基因,其在run藜苜蓿根中的表达被水泡-丛枝菌根(VAM)真菌定植和磷酸盐营养抑制。

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摘要

A cDNA clone (Mt4) was isolated as a result of a differential screen to identify genes showing altered expression during the interaction between Medicago truncatula and the vesicular-arbuscular mycorrhizal (VAM) fungus Glomus versiforme. Mt4 represents a M. truncatula mRNA that contains numerous short open reading frames, the two longest of which are predicted to encode polypeptides of 51 amino acids each. One of these open reading frames shares a short region of identity with a phosphate starvation-inducible gene from tomato. Mt4 gene expression is regulated in response to colonization by mycorrhizal fungi: transcripts were detected in non-colonized roots and levels decreased in both M. truncatula and M. sativa (alfalfa) roots after colonizationby G. versiforme. Transcript levels also decreased during the incomplete interaction between G. versiforme and a M. sativa mycorrhizal minus (myc-) line, indicating that the down-regulation of this gene occurs early during the interaction between the fungus and its host plant. Phosphate levels in the nutrient media also affected the expression of the Mt4 gene: transcripts were present in the roots of plants grown under phosphate-deficient conditions, but were undetectable in the roots of plants grown under phosphate sufficient conditions. Furthermore, expression was only observed when plants were grown under nitrogen-sufficient conditions. Northern blot analyses indicated that Mt4 transcripts are present primarily in roots and barely detectable in stems or leaves. Thus, Mt4 represents a M. truncatula gene whose expression is regulated in response to both colonization by mycorrhizal fungi and to the phosphate status of the plant. Nucleotide sequence data have been submitted to the EMBL/GenBank/DDBJ databases under the accession number U75742.
机译:作为差异筛选的结果,分离了一个cDNA克隆(Mt4),以鉴定截短苜蓿和水泡-丛枝菌根(VAM)真菌Glomus versiforme之间相互作用时表达改变的基因。 Mt4代表截短支原体mRNA,它包含许多短的开放阅读框,预计其中两个最长的阅读框将各自编码51个氨基酸的多肽。这些开放阅读框之一与来自番茄的磷酸饥饿诱导基因共享短的同一性区域。 Mt4基因表达受到菌根真菌定殖的调节:在非定殖根中检测到转录本,而在被疣状菌定居后,截短芒和苜蓿(苜蓿)根中的转录水平均下降。在Ver.formeforme和紫花苜蓿菌根减(myc-)品系之间的不完全相互作用中,转录水平也降低,表明该基因的下调发生在真菌与其宿主植物之间的相互作用的早期。营养培养基中的磷酸盐水平也影响Mt4基因的表达:转录物存在于缺磷条件下生长的植物根中,但在含磷条件下生长的植物根中却未检测到。此外,仅当植物在氮充足的条件下生长时才观察到表达。 Northern印迹分析表明,Mt4转录本主要存在于根中,而在茎或叶中几乎检测不到。因此,Mt4代表截短支原体基因,其表达受菌根真菌定植和植物磷酸盐状态的调节。核苷酸序列数据已以登录号U75742提交至EMBL / GenBank / DDBJ数据库。

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