山东农业大学学报(自然科学版)
山東農業大學學報(自然科學版)
산동농업대학학보(자연과학판)
JOURNAL OF SHANDONG AGRICULTURAL UNIVERSITY(NATURAL SCIENCE)
2015年
4期
481-486
,共6页
赵军林%丛红滋%苏长跃%于喜艳%王秀峰
趙軍林%叢紅滋%囌長躍%于喜豔%王秀峰
조군림%총홍자%소장약%우희염%왕수봉
甜瓜%PDS基因%克隆%表达
甜瓜%PDS基因%剋隆%錶達
첨과%PDS기인%극륭%표체
Cucumis melo L.%PDS gene%cloning%expression
以甜瓜自交系‘M01-3’果实cDNA为模板,采用RT-PCR和RACE技术,克隆了甜瓜果实八氢番茄红素脱氢酶(PDS)基因cDNA全长序列,命名为CmPDS(基因注册号:KC507802)。序列分析表明,该基因有开放阅读框1731 bp,编码576个氨基酸,与其他植物PDS氨基酸序列具有较高的同源性,尤其与黄瓜、南瓜、苦瓜PDS氨基酸序列高达92.6%~87.8%。荧光定量分析表明,该基因在甜瓜不同器官中均有表达,在叶片和授粉后25 d的果实中表达量较高,在根中表达量最低;随果实发育成熟,该基因表达量呈现先升高后降低趋势。
以甜瓜自交繫‘M01-3’果實cDNA為模闆,採用RT-PCR和RACE技術,剋隆瞭甜瓜果實八氫番茄紅素脫氫酶(PDS)基因cDNA全長序列,命名為CmPDS(基因註冊號:KC507802)。序列分析錶明,該基因有開放閱讀框1731 bp,編碼576箇氨基痠,與其他植物PDS氨基痠序列具有較高的同源性,尤其與黃瓜、南瓜、苦瓜PDS氨基痠序列高達92.6%~87.8%。熒光定量分析錶明,該基因在甜瓜不同器官中均有錶達,在葉片和授粉後25 d的果實中錶達量較高,在根中錶達量最低;隨果實髮育成熟,該基因錶達量呈現先升高後降低趨勢。
이첨과자교계‘M01-3’과실cDNA위모판,채용RT-PCR화RACE기술,극륭료첨과과실팔경번가홍소탈경매(PDS)기인cDNA전장서렬,명명위CmPDS(기인주책호:KC507802)。서렬분석표명,해기인유개방열독광1731 bp,편마576개안기산,여기타식물PDS안기산서렬구유교고적동원성,우기여황과、남과、고과PDS안기산서렬고체92.6%~87.8%。형광정량분석표명,해기인재첨과불동기관중균유표체,재협편화수분후25 d적과실중표체량교고,재근중표체량최저;수과실발육성숙,해기인표체량정현선승고후강저추세。
A full-length cDNA encoding Phytoene desaturase(PDS), named as CmPDS (GenBank:KC507802), was isolated from the fruit of‘M01-3’of Muskmelon(Cucumis melo L.) by RT-PCR and RACE. The cDNA has an open reading frame of 1731 bp and encodes a polypeptide of 576 amino acids. Sequence analysis showed that deduced CmPDS protein was highly homologous to other PDS proteins from different species, especially with Cucurbita moschata, Momordica charantia and Ricinus communis, that the identity of amino acid sequence was up to 92.6%~87.8%. Real time PCR analysis indicated that CmPDS expressed in different organs. The transcription levels of CmPDS in leaves and fruit of 25 d after pollination were higher than that in stems, roots and tubers respectively. With the development of fruit, the expression of the gene rised but reduced in the end.