首页 | 本学科首页   官方微博 | 高级检索  
     检索      

草莓果实中FaSAMDC基因的克隆、生物信息学及表达分析
引用本文:于晓阳,沈元月.草莓果实中FaSAMDC基因的克隆、生物信息学及表达分析[J].北京农学院学报,2017,32(3).
作者姓名:于晓阳  沈元月
作者单位:农业应用新技术北京市重点实验室/北京农学院植物科学技术学院,北京,102206;农业应用新技术北京市重点实验室/北京农学院植物科学技术学院,北京,102206
基金项目:北京市自然科学基金资助项目,科技北京百名领军人才培养计划
摘    要:【目的】为明确S-腺苷甲硫氨酸脱羧酶(SAMDC)在非呼吸跃变型草莓果实成熟中的作用。【方法】以‘北农香’草莓果实为试验材料,首先通过RT-PCR克隆FaSAMDC基因,其次通过SqRT-PCR分析发育果实(小绿、大绿、褪绿、白果、片红、全红)中的FaSAMDC基因的表达量。【结果】结果表明,FaSAMDC基因含有1 116bp开放阅读框,编码371个氨基酸,含有典型的脱羧酶保守功能结构域。随着草莓的果实发育,FaSAMDC表达量呈明显下降趋势并且在白果时期达到最低值,此后随着果实着色,表达量迅速上升并且成熟期达到最高。【结论】以上研究结果证实,S-腺苷甲硫氨酸脱羧酶可能参与草莓果实的成熟调控。

关 键 词:草莓果实  S-腺苷甲硫氨酸脱羧酶  基因克隆  半定量分析

Cloning,bioinformatics and expression analysis of FaSAMDC gene in strawberry fruits
YU xiaoyang,SHEN Yuanyue.Cloning,bioinformatics and expression analysis of FaSAMDC gene in strawberry fruits[J].Journal of Beijing Agricultural College,2017,32(3).
Authors:YU xiaoyang  SHEN Yuanyue
Abstract:Objective] To clarify the role of S-adenosylmethionine decarboxylase (SAMDC) in fruit ripening of non-climacteric strawberry.Methods]The fruit of ‘Beinongxiang'strawberry fruit was used as material,the FaSAMDC gene was cloned by RT-PCR,and the mRNA expression levels of FaSAMDC gene in developmental fruits were studied by SqRT-PCR including the stages small green (SG),big green (BG),de-greening (DG),white (Wt),partial red (PR),full red (FR)].Results]The results showed that,FaSAMDC gene contains an open reading frame of 1 116 bp,encoding 371 amino acids,typically containing decarboxylase conserved functional domains.During the fruit development of strawberry,the expression of FaSAM-DC showed a decreasing trend and reached the lowest value in the white period;then,with the fruit coloring,the expression level increased rapidly and reached the highest level at full red stage.Conclusion]These results suggested that S-adenosylmethionine decarboxylase may be involved in the regulation of strawberry fruit ripening.
Keywords:strawberry fruit  S-adenosylmethionine decarboxylase  gene cloning  Semi-quantitative analysis
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号