林业科学
林業科學
임업과학
SCIENTIA SILVAE SINICAE
2010年
2期
32-38
,共7页
安新民%王冬梅%王泽亮%王静澄%曹冠琳%薄文浩%张志毅
安新民%王鼕梅%王澤亮%王靜澄%曹冠琳%薄文浩%張誌毅
안신민%왕동매%왕택량%왕정징%조관림%박문호%장지의
毛白杨%PtLFY%表达模式%花芽%形态分化%qRT-PCR
毛白楊%PtLFY%錶達模式%花芽%形態分化%qRT-PCR
모백양%PtLFY%표체모식%화아%형태분화%qRT-PCR
Populus tomentosa%PtLFY%expression profiling%floral buds%morphological differentiation%qRT-PCR
以毛白杨花芽为材料,采用RT-PCR技术分离克隆毛白杨PtLFY cDNA序列,测序结果表明该序列全长1 314 bp,包含1个开放阅读框,编码377个氨基酸.Alignment分析显示该基因与拟南芥等物种LFY/FLO同源基因所编码的氨基酸相似性达到68%~75%.蛋白结构预测分析表明,在PtLFY蛋白N-端和C-端具有2个高度保守的区域,其中PtLFY-C端由7个α-helix组成Helix-turn-helix结构.采用Real-time qRT-PCR技术检测PtLFY在雌雄花芽发育过程中的表达模式,结果显示从9月13日到翌年1月25 Et,PtLFY在毛白杨雌雄花芽中持续稳定表达,到2月25日表达量少许下调,但该基因在雄花芽中的相对表达量明显高于雌花芽.解剖分析结果表明,雄花芽形态分化进程明显早于雌花芽,这种差异可能与PtLFY在雌雄花芽发育过程的差异表达存在密切联系.研究结果对于阐明PtLFY在毛白杨雌雄花芽发育和开花中的分子作用机制具有重要的理论意义,为进一步开展毛白杨开花调控研究奠定基础.
以毛白楊花芽為材料,採用RT-PCR技術分離剋隆毛白楊PtLFY cDNA序列,測序結果錶明該序列全長1 314 bp,包含1箇開放閱讀框,編碼377箇氨基痠.Alignment分析顯示該基因與擬南芥等物種LFY/FLO同源基因所編碼的氨基痠相似性達到68%~75%.蛋白結構預測分析錶明,在PtLFY蛋白N-耑和C-耑具有2箇高度保守的區域,其中PtLFY-C耑由7箇α-helix組成Helix-turn-helix結構.採用Real-time qRT-PCR技術檢測PtLFY在雌雄花芽髮育過程中的錶達模式,結果顯示從9月13日到翌年1月25 Et,PtLFY在毛白楊雌雄花芽中持續穩定錶達,到2月25日錶達量少許下調,但該基因在雄花芽中的相對錶達量明顯高于雌花芽.解剖分析結果錶明,雄花芽形態分化進程明顯早于雌花芽,這種差異可能與PtLFY在雌雄花芽髮育過程的差異錶達存在密切聯繫.研究結果對于闡明PtLFY在毛白楊雌雄花芽髮育和開花中的分子作用機製具有重要的理論意義,為進一步開展毛白楊開花調控研究奠定基礎.
이모백양화아위재료,채용RT-PCR기술분리극륭모백양PtLFY cDNA서렬,측서결과표명해서렬전장1 314 bp,포함1개개방열독광,편마377개안기산.Alignment분석현시해기인여의남개등물충LFY/FLO동원기인소편마적안기산상사성체도68%~75%.단백결구예측분석표명,재PtLFY단백N-단화C-단구유2개고도보수적구역,기중PtLFY-C단유7개α-helix조성Helix-turn-helix결구.채용Real-time qRT-PCR기술검측PtLFY재자웅화아발육과정중적표체모식,결과현시종9월13일도익년1월25 Et,PtLFY재모백양자웅화아중지속은정표체,도2월25일표체량소허하조,단해기인재웅화아중적상대표체량명현고우자화아.해부분석결과표명,웅화아형태분화진정명현조우자화아,저충차이가능여PtLFY재자웅화아발육과정적차이표체존재밀절련계.연구결과대우천명PtLFY재모백양자웅화아발육화개화중적분자작용궤제구유중요적이론의의,위진일보개전모백양개화조공연구전정기출.
A full-length cDNA denominated PtLFY was obtained from Populus tomentosa using RT-PCR technique.PtLFY is 1 314 bp and contains an open reading frame encoding a 377 amino acid polypeptide.Sequence analysis by blast showed that PtLFY shares 68%-75% homology in amino acid sequence with that encoded by Arobidopsis LFY and other species LFY/FLO homologues.It was found that PtLFY protein contains 2 conserved domains at N-terminal and C-terminal by alignment analysis.PtLFY-C region consists of a seven-α helix fold structure that binds target promoter DNA elements.The expression patterns of PtLFY in developmental floral buds were examined using real-time quantitative RT-PCR.The result showed that the continuous and stable transcripts of PtLFY were detected in both male and female floral buds of P.tomentosa from September 13 th to January 25 th,and then a slight decline was detected on February 25 th.The relative expression of PtLFY in male floral buds was obviously much higher than that in female floral buds.The anatomical results showed that initiation and differentiation of male floral buds were obviously earlier than female floral buds.It revealed that there is close relationship between expression of PtLFY and morphological difierentiation of floral buds in P.tomentosa.This study shed light on the molecular mechanism of PtLFY in development of both male and female floral buds and flowering in P.tomentosa,and the knowledge will benefit regulation of flowering.