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紫花苜蓿(黄花苜蓿)细胞冷驯化特异性基因cas18的cDNA序列、表达及转录稳定性

cDNA sequence, expression, and transcript stability of a cold acclimation-specific gene, cas18, of alfalfa (Medicago falcata) cells.

作者信息

Wolfraim L A, Langis R, Tyson H, Dhindsa R S

机构信息

Department of Biology, McGill University, Montreal, Quebec, Canada.

出版信息

Plant Physiol. 1993 Apr;101(4):1275-82. doi: 10.1104/pp.101.4.1275.

DOI:10.1104/pp.101.4.1275
PMID:8310062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC160650/
Abstract

The nucleotide sequence of a full-length cDNA, the deduced amino acid sequence, and the regulation of expression of a cold acclimation-specific gene, cas18, in cell suspension cultures of a freezing-tolerant cultivar of alfalfa (Medicago falcata cv Anik) have been determined. The deduced polypeptide, CAS18, is relatively small (17.6 kD), is highly hydrophilic, is rich in glycine and threonine, and contains two distinctive repeat elements. It exhibits homology with members of the LEA/RAB/dehydrin family of proteins, which accumulate in response to abscisic acid (ABA) or water stress. It is intriguing that cas18 is induced by neither ABA nor water stress. The cas18 cDNA hybridizes to three transcripts of 1.6, 1.4, and 1.0 kb, and the cDNA characterized here corresponds to the 1.0-kb transcript. The expression of this gene is about 30-fold greater in cold-acclimated cells than in nonacclimated cells. Although the accumulation of transcripts during cold acclimation is relatively slow, their disappearance during deacclimation is dramatically rapid, becoming undetectable in less than 5 h. Studies of nuclear run-on transcription show that cold acclimation enhances the transcription of this gene nearly 9-fold. The stability of cas18-detectable transcripts during deacclimation is considerably increased if transcription is inhibited with cordycepin. It therefore appears that low temperature regulates the expression of cas18 at both the transcriptional and posttranscriptional levels.

摘要

已确定了苜蓿(黄花苜蓿品种Anik)耐冻品种细胞悬浮培养物中一个全长cDNA的核苷酸序列、推导的氨基酸序列以及冷驯化特异性基因cas18的表达调控情况。推导的多肽CAS18相对较小(17.6 kD),高度亲水,富含甘氨酸和苏氨酸,并包含两个独特的重复元件。它与LEA/RAB/脱水素蛋白家族成员具有同源性,这些蛋白在脱落酸(ABA)或水分胁迫下积累。有趣的是,cas18既不受ABA诱导,也不受水分胁迫诱导。cas18 cDNA与1.6、1.4和1.0 kb的三种转录本杂交,此处表征的cDNA对应于1.0 kb的转录本。该基因在冷驯化细胞中的表达比未驯化细胞高约30倍。尽管冷驯化过程中转录本的积累相对较慢,但在去驯化过程中它们的消失却非常迅速,在不到5小时内就变得无法检测到。核运行转录研究表明,冷驯化使该基因的转录增强了近9倍。如果用放线菌素D抑制转录,在去驯化过程中可检测到的cas18转录本的稳定性会显著增加。因此,低温似乎在转录和转录后水平上都调节着cas18的表达。

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