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Cloning and characterization of a FLORICAULA/LEAFY ortholog, PFL, in polygamous papaya 被引量:4
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作者 Qingyi YU Paul H. MOORE +2 位作者 Henrik H. ALBERT Adrienne H.K. ROADER Ray MING 《Cell Research》 SCIE CAS CSCD 2005年第8期576-584,共9页
The homologous genes FLORICAULA (FLO) in Antirrhinum and LEAFY (LFY) in Arabidopsis are known to regu- late the initiation of flowering in these two distantly related plant species. These genes are necessary also for ... The homologous genes FLORICAULA (FLO) in Antirrhinum and LEAFY (LFY) in Arabidopsis are known to regu- late the initiation of flowering in these two distantly related plant species. These genes are necessary also for the expression of downstream genes that control floral organ identity. We used Arabidopsis LFY cDNA as a probe to clone and sequence a papaya ortholog of LFY, PFL. It encodes a protein that shares 61% identity with the Arabidopsis LFY gene and 71% identity with the LFY homologs of the two woody tree species: California sycamore (Platanus racemosa) and black cottonwood (Populus trichocarpa). Despite the high sequence similarity within two conserved regions, the N-terminal proline-rich motif in papaya PFL differs from other members in the family. This difference may not affect the gene function of papaya PFL, since an equally divergent but a functional LFY ortholog NEEDLY of Pinus radiata has been reported. Genomic and BAC Southern analyses indicated that there is only one copy of PFL in the papaya genome. In situ hybridization experiments demonstrated that PFL is expressed at a relatively low level in leaf primordia, but it is expressed at a high level in the floral meristem. Quantitative PCR analyses revealed that PFL was expressed in flower buds of all three sex types - male, female, and hermaphrodite with marginal difference between hermaphrodite and unisexual flowers. These data suggest that PFL may play a similar role as LFY in flower development and has limited effect on sex differentiation in papaya. 展开更多
关键词 无性繁殖 同源基因 金鱼草属植物 植物叶部 植物种类
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蝴蝶兰Ph SVP的克隆及其在花发育过程中的表达分析 被引量:5
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作者 张燕 许申平 +4 位作者 梁芳 蒋素华 袁秀云 牛苏燕 崔波 《园艺学报》 CAS CSCD 北大核心 2020年第6期1111-1125,共15页
从蝴蝶兰杂交品种‘大辣椒’中克隆到SVP同源MADS-box基因PhSVP,使用RACE方法获得PhSVP全长,其开放阅读框为687 bp,编码228个氨基酸。蛋白序列多重比对表明PhSVP蛋白包含一个高度保守的MEF2-like MADS结构域和一个中度保守的K-box结构域... 从蝴蝶兰杂交品种‘大辣椒’中克隆到SVP同源MADS-box基因PhSVP,使用RACE方法获得PhSVP全长,其开放阅读框为687 bp,编码228个氨基酸。蛋白序列多重比对表明PhSVP蛋白包含一个高度保守的MEF2-like MADS结构域和一个中度保守的K-box结构域,且与兰科的SVP/AGL24同源蛋白相似度高,进化树分析也表明PhSVP蛋白与其他兰科植物的SVP/AGL24同源蛋白亲缘关系最近。PhSVP的空间表达模式表明其在营养器官表达量高,在萼片、侧瓣和唇瓣等生殖器官表达量低。进一步对PhSVP在成花转换和花发育过程中花序顶端的表达进行分析,表明PhSVP的转录水平在营养分生组织向花序分生组织过渡的过程中无显著变化,仅在花序分生组织阶段有少量上升,但在花发育早期花分生组织阶段中的表达水平显著升高,而在花发育后期的萼片原基、花瓣原基和合蕊柱原基阶段持续下降。此外还发现A类基因PhAP1在花发育过程中的花序顶端的表达模式与PhSVP相似,而B类基因PhPI和C类基因PhAG在花瓣原基和合蕊柱原基阶段的表达量最高。检测了PhSVP在抽葶期、花蕾期和盛花期的根、叶和花葶中的转录水平,结果表明PhSVP在花蕾期的根中的表达量稍高于其他时期,在不同阶段的叶中的表达水平无显著差异,而在抽葶期花葶中的表达量显著高于花蕾期和盛花期。试验结果暗示蝴蝶兰PhSVP可能起到调控花分生组织状态的维持、避免花器官原基过早分化的作用。 展开更多
关键词 蝴蝶兰 SVP基因 表达分析 花发育 花分生组织决定
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