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Isolation and Characterization of a Small Heat Shock Protein Gene from Maize

机译:玉米小热激蛋白基因的分离与鉴定

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摘要

A maize (Zea mays L.) genomic clone (Zmempr 9′) was isolated on the basis of its homology to a meiotically expressed Lilium sequence. Radiolabeled probe made from the maize genomic clone detected complementary RNA at high fidelity. Furthermore, it hybridized to RNA isolated from staged (an interval that is coincident with meiotic prophase) maize tassel spikelets. Complimentary RNA was strongly (at least 50-fold) induced during heat shock of maize somatic tissue and appeared as a single size class in Northern blot hybridizations. Sequencing of the complete coding region of Zmempr 9′ confirmed the homology of the inferred amino acid sequence to other small heat shock proteins. Consensus sequences found in the flanking regions corresponded to the usual signals for initiation of RNA transcription, polyadenylate addition, and the induction of heat shock genes. The latter sequences conferred heat shock-specific transient expression in electroporated protoplasts when cloned into promoterless reporter gene plasmid constructs. Hybrid-selected translations revealed specific translation products ranging from 15 to 18 kilodaltons, providing evidence that this gene is a member of a related multigene family. We therefore conclude that this maize genomic DNA clone, recovered through its homology to clones for meiotic transcripts in lily, represents a genuine maize small heat shock protein gene.
机译:基于其与减数分裂表达的百合属植物序列的同源性,分离了玉米(Zea mays L.)基因组克隆(Zmempr 9')。由玉米基因组克隆制成的放射性标记探针可高保真检测互补RNA。此外,它与从分阶段(与减数分裂前期相一致的间隔)玉米流苏小穗分离的RNA杂交。在玉米体细胞组织热激过程中,强烈诱导了互补RNA(至少50倍),并在RNA印迹杂交中显示为单个大小类别。 Zmempr 9'的完整编码区的测序证实了推断的氨基酸序列与其他小热激蛋白的同源性。在侧翼区域中发现的共有序列对应于RNA转录起始,聚腺苷酸添加和热休克基因诱导的通常信号。当克隆到无启动子的报告基因质粒构建体中时,后一序列赋予电穿孔原生质体热休克特异性瞬时表达。杂种选择的翻译揭示了15到18道尔顿之间的特定翻译产物,提供了该基因是相关多基因家族成员的证据。因此,我们得出的结论是,该玉米基因组DNA克隆通过与百合中减数分裂转录本克隆的同源性恢复,代表了真正的玉米小热激蛋白基因。

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