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八肋游仆虫一个新β-微管蛋白基因的克隆与序列分析

Cloning and Sequence Analysis of a Novel β-tubulin Gene from Euplotes octocarinatus

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【作者】 柴宝峰王景涛梁爱华

【Author】 CHAI Bao-feng1,WANG Jing-tao2,LIANG Ai-hua1 (1.Institute of Biotechnology,Shanxi University,Taiyuan 030006; 2.Institute of Loess Plateau,Shanxi University,Taiyuan 030006,China)

【机构】 山西大学生物技术研究所山西大学黄土高原研究所山西大学生物技术研究所 山西太原030006山西太原030006

【摘要】 从八肋游仆虫细胞中克隆到一种新的β-微管蛋白基因.序列分析结果表明:在大核中,该基因全长1561bp.与已经报道过的β-微管蛋白基因不同,它的5′端基因上游调控序列有49 bp,AT含量为75.5%.上游调控序列中仅有一个TATAA框,没有CCAAT框;该基因的3′端的下游调控序列有121 bp,富含AT碱基,达到86.8%,其中有明显的反向重复序列.上下游调控序列中各有一个断裂信号TTGAA和TTCAA,负责从小核到大核发育过程中大核染色体的形成.从小核基因组中克隆到相应的基因片段,比大核中的序列多7个碱基5′-CATGCTC-3′,其功能尚不清楚.序列比对表明,新的β-微管蛋白基因与已经报道的β-微管蛋白基因的同源性92.3%,阅读框中有2个氨基酸的变化,将它命名为β2-微管蛋白基因.

【Abstract】 A novel β-tubulin gene was cloned from the cell of Euplotes octocarinatus.The gene from macronuclear DNA was 1561 bp in length,including non-coding regions and telomeric sequences at both ends.Different from reported β-tubulin gene,5′non-coding regions was 49 bp in length,abundance in AT(75.5 %),containing a TATAA-box.3′-noncoding regions was 121 bp length,abundance in AT reaching to 86.8 %,containing two standard reverse repeat sequences.A break signal TTGAA and TTCAA appeared in 5′ and 3′ non-coding regions,17 bp away from initiate codon and stop codon,which were responsible for development of chromosome in macronucleus that formed from micronucleus through breakage process.The new β-tubulin gene cloned from micronuclear DNA had a additional small sequences 5′-CATGCTC-3′,which function was unclear.The result of BLAST in NCBI demonstrated that the new β-tubulin gene shared a homology of 92.3 % with reported β-tubulin gene.The new β-tubulin gene was named as β2-tubulin.

【关键词】 β-微管蛋白基因克隆非编码区
【Key words】 Euplotes octocarinatusβ-tubulingene colning
【基金】 国家自然科学基金(30270239,30670282);山西自然科学基金(20041079,20051065)
  • 【文献出处】 山西大学学报(自然科学版) ,Journal of Shanxi University(Natural Science Edition) , 编辑部邮箱 ,2007年02期
  • 【分类号】Q78
  • 【被引频次】5
  • 【下载频次】102
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