琯溪蜜柚汁胞粒化过程中基因差别表达cDNA的克隆及序列分析
cDNA Cloning in Gene Differential Display and its Sequence Analysis of Citrus guanxi-miyou Fruit Juicy Sac in Process of Granulation
本研究以琯溪蜜柚果肉汁胞为材料,运用RT-PCR的方法,得到了琯溪蜜柚果实汁胞粒化过程中未粒化汁胞的差异片断,通过Blast分析发现该片段序列与从发育中桃果实分离得到的cDNA有高度的同源性。在此基础上,通过5′-RACE获得该cDNA的5′末端序列,经序列分析、比对和拼接,得到该cDNA全序列。并对得到的序列进行了一些分析,从分子生物学角度对粒化的研究做了初步的探索。结果表明:琯溪蜜柚汁胞基因差别表达cDNA全长1152bp,包含1个819bp的开放阅读框架,编码272个氨基酸。进一步的Blast分析显示,该cDNA与20S蛋白质酶体的β亚基5高度同源。其中,与菠菜的20S蛋白质酶体的β亚基5同源性最高,为83.09%,与水稻、小麦的同源性分别为74.73%和73.12%。
Guanxi-miyou fruit being taken as experimental material in this study, CDNA difference fragment of non-granulated juicy sac was isolated in the process of granulation of Guangxi-miyou by reverse transcription-polymerase chain reaction (RT- PCR). It was found that the Guanxi-miyou CDNA fragment was significantly homologous to developing pear fruit’s by Blast analysis. The 5’ end sequence was also found by 5’ RACE , and then the full length of CDNA given by sequence analysis, Blast and joining was analyzed, and the primary exploration on granulation was made in prospective of biology. The result showed that the full length of cDNA in Guangxi-miyou juicy sac was an open reading frame of 1152 bp including one ORF with 819 bp, and 272 amino acid sequence. The further Blast analysis showed that CDNA had highly homologous to 20S proteasome beta subunit, among which 83.09% of homology to spinach’ was highest, 74.73% to rice’ and 73.12% to wheat’ respectively.
潘东明、林琳、佘文琴、郭志雄
分子生物学植物学农艺学
琯溪蜜柚基因差别cDNA序列分析同源性分析
itrus guanxi-miyouDifferential displayGranulationSequencingHomologous analysis
潘东明,林琳,佘文琴,郭志雄.琯溪蜜柚汁胞粒化过程中基因差别表达cDNA的克隆及序列分析[EB/OL].(2008-01-09)[2025-08-04].http://www.paper.edu.cn/releasepaper/content/200801-279.点此复制
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