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三个编码脂质转移蛋白的大麦基因的发育及病原体诱导表达

Developmental and pathogen-induced expression of three barley genes encoding lipid transfer proteins.

作者信息

Molina A, García-Olmedo F

机构信息

Laboratorio de Bioquímica y Biología Molecular, ETS Ingenieros Agrónomos-UPM, Madrid, Spain.

出版信息

Plant J. 1993 Dec;4(6):983-91. doi: 10.1046/j.1365-313x.1993.04060983.x.

Abstract

Clones for three barley non-specific lipid transfer proteins (LTP2, LTP3, and LTP4; formerly Cw18, Cw20 and Cw21, respectively) which had been previously shown to inhibit growth of plant pathogens, were selected and characterized from a cDNA library derived from young etiolated leaves. Genes Ltp2 and Ltp4 were located in chromosome 3H and gene Ltp3 was assigned to chromosome 7H by Southern blot analysis of wheat-barley disomic addition lines, using gene-specific probes (3'-ends of cDNAs). These assignments were confirmed by the polymerase chain reaction, using specific primers. The three genes were expressed in stem, shoot apex, leaves and roots (at low levels) throughout development. Genes Ltp3 and Ltp4 were expressed at high levels, and Lpt2 at low levels, in the spike (rachis, lemma plus palea and grain coats). Neither of the mRNAs was detected in endosperm. The proteins were localized by tissue-printing with polyclonal antibodies in the outer cell layer of the exposed surfaces of the plant, throughout the embryo, and in vascular tissues. Expression levels in leaves were moderately increased by 0.34 M NaCl and by 0.1 mM abscisic acid and were not affected by cold, drought, salicylate, 2,6-dichloro-isonicotinic acid, ethylene or ethephon. Methyl Jasmonate (10 microM) switched off all three genes. Inoculation with Av6 or vir6 isolates of the fungal pathogen Erysiphe graminis increased the three mRNAs, especially that of LTP4, which reached a maximum nine-fold increase 12-16 h after infection.

摘要

从来源于黄化幼叶的cDNA文库中筛选并鉴定了三个大麦非特异性脂质转移蛋白(LTP2、LTP3和LTP4;以前分别称为Cw18、Cw20和Cw21)的克隆,这些蛋白先前已被证明可抑制植物病原体的生长。通过使用基因特异性探针(cDNA的3'末端)对小麦-大麦二体附加系进行Southern印迹分析,将Ltp2和Ltp4基因定位在3H染色体上,Ltp3基因定位在7H染色体上。使用特异性引物通过聚合酶链反应证实了这些定位。这三个基因在整个发育过程中在茎、茎尖、叶和根中(低水平)表达。Ltp3和Ltp4基因在穗(穗轴、内外稃和种皮)中高水平表达,Lpt2基因低水平表达。在胚乳中未检测到任何一种mRNA。通过用多克隆抗体进行组织印迹,发现这些蛋白定位于植物暴露表面的外层细胞层、整个胚以及维管组织中。叶片中的表达水平在0.34 M NaCl和0.1 mM脱落酸处理下适度增加,不受寒冷、干旱、水杨酸、2,6-二氯异烟酸、乙烯或乙烯利的影响。茉莉酸甲酯(10 microM)使所有三个基因关闭。用真菌病原体禾白粉菌的Av6或vir6分离株接种可增加这三种mRNA的表达,尤其是LTP4的mRNA,在感染后12 - 16小时达到最大增加九倍。

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