首页> 美国卫生研究院文献>The EMBO Journal >Molecular analysis of two phytohemagglutinin genes and their expression in Phaseolus vulgaris cv. Pinto a lectin-deficient cultivar of the bean
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Molecular analysis of two phytohemagglutinin genes and their expression in Phaseolus vulgaris cv. Pinto a lectin-deficient cultivar of the bean

机译:两个植物血凝素基因的分子分析及其在菜豆中的表达Pinto豆中缺乏凝集素的品种

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摘要

Phytohemagglutinin (PHA), the seed lectin of the common bean, Phaseolus vulgaris, is encoded by two highly homologous, tandemly linked genes, dlec1 and dlec2, which are coordinately expressed at high levels in developing cotyledons. Their respective transcripts translate into closely related polypeptides, PHA-E and PHA-L, constituents of the tetrameric lectin which accumulates at high levels in developing seeds. In the bean cultivar Pinto UI111, PHA-E is not detectable, and PHA-L accumulates at very reduced levels. To investigate the cause of the Pinto phenotype, we cloned and sequenced the two PHA genes of Pinto, called Pdlec1 and Pdlec2, and determined the abundance of their respective mRNAs in developing cotyledons. Both genes are more than 90% homologous to the normal PHA genes found in other cultivars. Pdlec1 carries a 1-bp frameshift mutation close to the 5' end of its coding sequence. Only very truncated polypeptides could be made from its mRNA. The gene Pdlec2 encodes a polypeptide, which resembles PHA-L and its predicted amino acid sequence agrees with the available Pinto PHA amino acid sequence data. Analysis of the mRNA of developing cotyledons revealed that the Pdlec1 message is reduced 600-fold, and Pdlec2 mRNA is reduced 20-fold with respect to mRNA levels in normal cultivars. A comparison of the sequences which are upstream from the coding sequence shows that Pdlec2 has a 100-bp deletion compared to the other genes (dlec1, dlec2 and Pdlec1). This deletion which contains a large tandem repeat may be responsible for the low level of expression of Pdlec2. The very low expression of Pdlec1 is as yet unexplained.
机译:植物血凝素(PHA)是普通豆菜豆的种子凝集素,由两个高度同源,串联的基因dlec1和dlec2编码,它们在子叶中以高水平协同表达。它们各自的转录本翻译成紧密相关的多肽PHA-E和PHA-L,它们是四聚植物凝集素的成分,四聚植物凝集素在发育中的种子中大量积累。在大豆品种Pinto UI111中,无法检测到PHA-E,并且PHA-L的积累非常低。为了研究Pinto表型的原因,我们克隆并测序了Pinto的两个PHA基因,分别称为Pdlec1和Pdlec2,并确定了它们各自在子叶发育中的mRNA的丰度。这两个基因与在其他品种中发现的正常PHA基因有90%以上的同源性。 Pdlec1在其编码序列的5'末端附近带有一个1-bp移码突变。从其mRNA只能截短的多肽。 Pdlec2基因编码的多肽类似于PHA-L,其预测的氨基酸序列与可用的Pinto PHA氨基酸序列数据一致。对发育中子叶的mRNA的分析显示,相对于正常品种的mRNA水平,Pdlec1信息减少了600倍,Pdlec2 mRNA减少了20倍。对编码序列上游序列的比较显示,与其他基因(dlec1,dlec2和Pdlec1)相比,Pdlec2具有100 bp的缺失。包含大量串联重复的缺失可能是Pdlec2表达水平低的原因。尚无法解释Pdlec1的极低表达。

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