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[脱落酸对铁皮石斛中转录活跃的Ty1-copia反转录转座子的影响]

[Effect of ABA on transcriptionally active Ty1-copia retrotransposons in Dendrobium officinale].

作者信息

Li Cong, Si Jin-Ping, Gao Yan-Hui, Zhu Yu-Qiu, Jiang Yuan

出版信息

Zhongguo Zhong Yao Za Zhi. 2014 May;39(10):1788-94.

Abstract

Using universal primer Tyl-copia retrotransposon RT, the conserved reverse transcriptase domain of about 260 bp was amplified by RT-PCR from the Dendrobium officinale which induced by 100 micromol x L(-1) abscisic acid (ABA), indicating these retrotransposons activated by 100 micromol x L(-1) ABA. The amplicons were recovered and cloned,then sequenced and analyzed by related bioinformatics software. Forty-two Ty1-copia like retrotransposon RT transcriptionally activated were obtained with high heterogeneity. The length of these sequences varied from 247 to 266 bp, and was rich in AT and homology ranged from 46.3% to 98.9%. The same to Ty1-copia like retrotransposon RT of genome, different c/s-acting regulatory elements induced by stress conditions and the starting transcription signals, corresponding to CAAT box, TATA box conserved sequences and some other regulatory elements. The c/s-acting regulatory elements induced by stress conditions of reverse transcriptase transcriptionally activated of Tyl-copia retrotransposons were significantly increased than that of Ty1-copia like retrotransposon RT of genome. When being translated into amino acids, fifteen sequences presented stop codon mutation, nineteen sequences presented frameshift mutation, and all sequences presented conserved sequence "SLYGKQ" mutation. Five categories were identified through phylogenic analysis after alignment analyses of their amino acid sequences, and with Ty1-copia like retrotransposon RT of genome having low homology, which indicated that reverse transcriptase transcriptionally activated of Ty1-copia retrotransposons which induced by ABA had Significantly differences with Ty1-copia like retrotransposon RT of genome.

摘要

使用通用引物Tyl-copia逆转录转座子RT,通过RT-PCR从经100微摩尔×L(-1)脱落酸(ABA)诱导的铁皮石斛中扩增出约260 bp的保守逆转录酶结构域,表明这些逆转录转座子被100微摩尔×L(-1) ABA激活。回收并克隆扩增产物,然后进行测序,并使用相关生物信息学软件进行分析。获得了42个转录激活的类Ty1-copia逆转录转座子RT,具有高度异质性。这些序列的长度在247至266 bp之间,富含AT,同源性在46.3%至98.9%之间。与基因组中的类Ty1-copia逆转录转座子RT相同,不同的顺式作用调控元件由胁迫条件诱导产生,起始转录信号对应于CAAT框、TATA框保守序列和其他一些调控元件。胁迫条件诱导的Tyl-copia逆转录转座子逆转录酶转录激活的顺式作用调控元件比基因组中的类Ty1-copia逆转录转座子RT显著增加。当翻译成氨基酸时,15个序列出现终止密码子突变,19个序列出现移码突变,所有序列均出现保守序列“SLYGKQ”突变。对其氨基酸序列进行比对分析后,通过系统发育分析鉴定出五类,与基因组中的类Ty1-copia逆转录转座子RT同源性较低,这表明ABA诱导的Ty1-copia逆转录转座子逆转录酶转录激活与基因组中的类Ty1-copia逆转录转座子RT存在显著差异。

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