Tonoike H, Han I S, Jongewaard I, Doyle M, Guiltinan M, Fosket D E
Department of Developmental and Cell Biology, University of California, Irvine 92717.
Plant J. 1994 Mar;5(3):343-51. doi: 10.1111/j.1365-313x.1994.00343.x.
The tubB1 beta-tubulin gene of Glycine max (previously named s beta 1) is highly expressed only in rapidly elongating regions of etiolated seedling hypocotyls and this expression is strongly downregulated when the seedlings are exposed to light. Primer extension demonstrated that the gene was transcribed in these tissues and contained two sites of transcriptional initiation. To determine the mechanism regulating tubB1 expression, a chimeric reporter gene was constructed by fusing 5' upstream regions of tubB1 to a promoterless beta-glucuronidase (GUS) gene and these constructs were introduced into protoplasts by electroporation. Strong transient expression of the reporter gene was obtained after electroporation of chimeric constructs containing 1 kb of tubB1 5' upstream sequence into tobacco protoplasts. Deletion of the distal most 300 bp from the 5' sequence of tubB1 enhanced expression, suggesting the possibility of a negative transcriptional regulator in this region. Additional deletions of the 5' sequence reduced expression substantially. Constructs containing a tubB1 3' terminus were expressed at much lower levels than those containing a nopaline synthase (NOS) 3' terminus. The tubB1-GUS chimeric gene also was introduced into tobacco by Agrobacterium-mediated Ti plasmid transformation and the organ-specific expression pattern of the chimeric gene was determined in seedlings of the transgenic plants. Hypocotyls exhibited strong GUS activity when the seedlings were germinated in darkness, but lacked the GUS enzyme when the seedlings were germinated in the light.(ABSTRACT TRUNCATED AT 250 WORDS)
大豆的tubB1β-微管蛋白基因(以前称为sβ1)仅在黄化幼苗下胚轴的快速伸长区域高表达,并且当幼苗暴露于光照时,这种表达会强烈下调。引物延伸表明该基因在这些组织中被转录,并且包含两个转录起始位点。为了确定调节tubB1表达的机制,通过将tubB1的5'上游区域与无启动子的β-葡萄糖醛酸酶(GUS)基因融合构建了嵌合报告基因,并通过电穿孔将这些构建体导入原生质体。将含有1kb tubB1 5'上游序列的嵌合构建体电穿孔导入烟草原生质体后,获得了报告基因的强瞬时表达。从tubB1的5'序列中删除最远端的300bp增强了表达,表明该区域可能存在负转录调节因子。5'序列的进一步缺失显著降低了表达。含有tubB1 3'末端的构建体的表达水平远低于含有胭脂碱合酶(NOS)3'末端的构建体。tubB1-GUS嵌合基因也通过农杆菌介导的Ti质粒转化被导入烟草,并在转基因植物的幼苗中确定了嵌合基因的器官特异性表达模式。当幼苗在黑暗中萌发时,下胚轴表现出强烈的GUS活性,但当幼苗在光照下萌发时,则缺乏GUS酶。(摘要截短至250字)