Tagu D, Walker N, Ruiz-Avila L, Burgess S, Martìnez-Izquierdo J A, Leguay J J, Netter P, Puigdomènech P
Departament de Genètica Molecular, CID-CSIC, Barcelona, Spain.
Plant Mol Biol. 1992 Nov;20(3):529-38. doi: 10.1007/BF00040611.
The expression of the maize gene coding for a hydroxyproline-rich glycoprotein (HRGP) has been studied by measuring the mRNA accumulation after wounding or ethylene treatment. RNA blot and in situ hybridization techniques have been used. The temporal and tissue-specific expression has been observed: the cells related to the vascular system show the more intense HRGP mRNA accumulation. Transcriptional constructions of the maize HRGP promoter have been tested on different maize tissues by microbombarding. A 582 bp promoter is able to direct the expression of the gus gene on calli and young leaves. Constructions having shorter promoter sequences lose this ability. The 582 bp construction retains the general specificity of expression observed for the HRGP gene.
通过测量受伤或乙烯处理后mRNA的积累,对编码富含羟脯氨酸糖蛋白(HRGP)的玉米基因的表达进行了研究。使用了RNA印迹和原位杂交技术。观察到了其时间和组织特异性表达:与维管系统相关的细胞显示出更强的HRGP mRNA积累。通过微粒轰击在不同玉米组织上测试了玉米HRGP启动子的转录构建体。一个582 bp的启动子能够指导gus基因在愈伤组织和幼叶上的表达。具有较短启动子序列的构建体失去了这种能力。582 bp的构建体保留了HRGP基因所观察到的一般表达特异性。