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海带CRY-DASH基因的克隆与转录表达分析

Cloning and transcriptional analysis of CRY-DASH from Saccharina japonica (Laminariales, Phaeophyceae)

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【作者】 李璐张朋艳姚建亭段德麟

【Author】 LI Lu;ZHANG Peng-yan;YAO Jian-ting;DUAN De-lin;Institute of Oceanology,Chinese Academy of Sciences;CAS Key Laboratory of Experimental Marine Biology,Institute of Oceanology,Chinese Academy of Sciences;Marine Biology and Biotechnology Laboratory,Pilot National Laboratory for Marine Science and Technology (Qingdao);University of Chinese Academy of Sciences;

【通讯作者】 段德麟;

【机构】 中国科学院海洋研究所中国科学院实验海洋生物学重点实验室青岛海洋科学与技术试点国家实验室实验海洋生物学与生物技术实验室中国科学院大学

【摘要】 利用cDNA末端快速克隆(RACE)技术,获得海带(Saccharina japonica) CRY-DASH基因(SjCRYDASH)全长序列,结构分析发现,其ORF区长1779 bp,编码592个氨基酸。进行氨基酸同源序列比对,其与其他藻类和高等植物间存在两个重要辅基MTHF和FAD结合的保守域。通过不同光质照射诱导海带幼孢子体,发现蓝光、白光诱导1h后,均能使SjCRY-DASH转录水平上升,且SjCRY-DASH对蓝光的响应更强烈。本研究结果为研究大型褐藻-海带CRY-DASH受光诱导调控功能打下基础。

【Abstract】 In the present work, we characterized the full-length cDNA of CRY-DASH from Saccharina japonica(designated as SjCRY-DASH) using the rapid amplification of cDNA ends technique. The open reading frame length of SjCRY-DASH was 1779 bp, and the gene encoded a protein of 592 amino acids. Using multiple alignments of protein sequences, conserved residues interacting with two crucial cofactors, MTHF and FAD, were detected between SjCRY-DASH and several DASH-type proteins of other algae and higher plants. Juvenile sporophytes were induced by light of different wavelengths. Both blue and white light upregulated the transcriptional level of SjCRY-DASH within 1 h, although the gene showed stronger responses to blue light than to white light. Our results lay a foundation for future studies on light induction and regulation by CRY-DASH of S. japonica.

【基金】 国家海洋公益性行业科研专项(201405040);青岛海洋科学与技术国家实验室计划项目(2015ASKJ02)~~
  • 【分类号】S917.3;Q943.2
  • 【下载频次】70
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