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鉴定一个指导大麦几丁质酶基因糊粉层特异性表达的增强子/沉默子序列。

Identification of an enhancer/silencer sequence directing the aleurone-specific expression of a barley chitinase gene.

作者信息

Leah R, Skriver K, Knudsen S, Ruud-Hansen J, Raikhel N V, Mundy J

机构信息

Carlsberg Research Laboratory, Copenhagen, Denmark.

出版信息

Plant J. 1994 Oct;6(4):579-89. doi: 10.1046/j.1365-313x.1994.6040579.x.

DOI:10.1046/j.1365-313x.1994.6040579.x
PMID:7987416
Abstract

Chitinases are expressed in various plant tissues where they are thought to play a role in defense against chitin-containing pathogens. Transient gene expression assays have been used in tissues of barley to delineate promoter sequences involved in the regulation of an aleurone-specific chitinase gene (Chi26), and of a vegetatively expressed chitinase gene (Chi33). The assays measured the activities of transcriptional fusions between chitinase 5' upstream sequences and GUS reporter genes after DNA delivery by particle bombardment. Analysis of Chi26 5' and 3' promoter deletions indicated that sequences between -200 and -140 confer developmental and aleurone-specific expression. Deletions/replacements covering this part of the promoter indicated that sequences between -179 and -147 (E-region) direct expression in aleurone cells. The ability of the 33bp E-region of the Chi26 promoter to activate transcription specifically in aleurone was confirmed by constructing and testing two types of chimeric promoters. The first type, which contained two copies of the E-region fused to the CaMV 35S TATA box, conferred aleurone-specific expression of a GUS reporter gene. The second type, which contained a single copy of the E-region inserted into a deleted, inactive Chi33 promoter derivative, was also capable of directing transcription in aleurone but not in leaves. The pattern of expression of this and other Chi26/Chi33 chimeric promoters suggest that the E-region contains cis-acting sequences which activate transcription in aleurone and silence transcription in leaves. DNA sequence motifs implicated in the regulation of Chi26 and Chi33 are described.

摘要

几丁质酶在多种植物组织中表达,据信它们在抵御含几丁质病原体的防御过程中发挥作用。瞬时基因表达分析已用于大麦组织中,以描绘参与调控糊粉层特异性几丁质酶基因(Chi26)和营养体表达的几丁质酶基因(Chi33)的启动子序列。这些分析通过微粒轰击递送DNA后,测量了几丁质酶5'上游序列与GUS报告基因之间转录融合的活性。对Chi26 5'和3'启动子缺失的分析表明,-200至-140之间的序列赋予发育和糊粉层特异性表达。覆盖启动子这一部分的缺失/替换表明,-179至-147之间的序列(E区)指导糊粉层细胞中的表达。通过构建和测试两种类型的嵌合启动子,证实了Chi26启动子的33bp E区在糊粉层中特异性激活转录的能力。第一种类型包含与CaMV 35S TATA框融合的两个E区拷贝,赋予GUS报告基因糊粉层特异性表达。第二种类型包含插入缺失的、无活性的Chi33启动子衍生物中的单个E区拷贝,也能够在糊粉层中指导转录,但不能在叶片中指导转录。这种和其他Chi26/Chi33嵌合启动子的表达模式表明,E区包含顺式作用序列,这些序列在糊粉层中激活转录并在叶片中使转录沉默。描述了与Chi26和Chi33调控相关的DNA序列基序。

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