Key Laboratory of Horticultural Plant Biology, Ministry of Education, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, People's Republic of China.
Plant Cell Rep. 2012 Oct;31(10):1851-65. doi: 10.1007/s00299-012-1299-8. Epub 2012 Jul 21.
The LEAFY/FLORICAULA (LFY/FLO) homologous genes are necessary for normal flower development in diverse angiosperm species. To understand the genetic and molecular mechanisms underlying floral initiation and development in Platanaceae, an early divergent eudicot family consisting of large monoecious trees, we isolated a homolog of LFY/FLO, PlacLFY, and its promoter from London plane (Platanus acerifolia). PlacLFY is 1,419 bp in length, with an ORF of 1,122 bp encoding a predicted polypeptide of 374 amino acids and 5'/3'-UTR of 54 and 213 bp, respectively. The putative PlacLFY protein showed a high degree of identity (56-84 %) with LFY/FLO homologs from other species, including two highly conserved regions, the N and C domains, and a less conserved amino-terminal proline-rich region. Real-time PCR analysis showed that PlacLFY was expressed mainly in male inflorescences from May of the first year to March of next year, with the highest expression level in December, and in female inflorescences from June to April of next year. PlacLFY mRNA was also detected strongly in subpetiolar buds of December from 4-year-old and adult trees, and slightly in stem of young seedling and young leaf of adult plant. Additionally, we cloned 1,138 bp promoter sequence of PlacLFY and we drove GUS expression in transgenic tobacco by the chimerical pPlacLFY::GUS construction. Histological GUS staining analysis indicated that PlacLFY promoter can drive GUS gene expression in shoot apex, stem, young leaf and petiole, flower stalk, petal tip, and young/semi-mature fruits of transgenic tobacco, which is almost identical to the expression pattern of PlacLFY in London plane. The results revealed that the PlacLFY gene isolated from London plane is expressed not only in reproductive organ but also in vegetative organs. Moreover, this expression pattern is consistent with the expression pattern in tobacco of a GUS reporter gene under the control of the potential promoter region of PlacLFY.
LEAFY/FLORICAULA (LFY/FLO) 同源基因对于不同的被子植物物种的正常花发育是必要的。为了理解在悬铃木科(Platanaceae)中花起始和发育的遗传和分子机制,该科是一个早期分化的真双子叶植物家族,由大型雌雄同株的树木组成,我们从伦敦悬铃木(Platanus acerifolia)中分离出 LFY/FLO 的同源物 PlacLFY 及其启动子。PlacLFY 的长度为 1419bp,ORF 为 1122bp,编码一个预测的 374 个氨基酸的多肽和 5'/3'-UTR 分别为 54 和 213bp。推测的 PlacLFY 蛋白与其他物种的 LFY/FLO 同源物具有高度的同一性(56-84%),包括两个高度保守的区域,N 和 C 结构域,以及一个不太保守的氨基末端富含脯氨酸的区域。实时 PCR 分析表明,PlacLFY 主要在雄性花序中表达,从第一年的 5 月到次年的 3 月,最高表达水平在 12 月,在雌性花序中从次年的 6 月到 4 月表达。PlacLFY mRNA 在 4 年生和成年树的 12 月叶柄芽中也强烈表达,在幼龄幼苗的茎和成年植物的幼叶中略有表达。此外,我们克隆了 PlacLFY 的 1138bp 启动子序列,并通过嵌合 pPlacLFY::GUS 构建驱动转基因烟草中的 GUS 表达。组织学 GUS 染色分析表明,PlacLFY 启动子可以在转基因烟草的茎尖、茎、幼叶和叶柄、花梗、花瓣尖端和幼果/半成熟果中驱动 GUS 基因表达,这与 PlacLFY 在伦敦悬铃木中的表达模式几乎相同。结果表明,从伦敦悬铃木中分离出的 PlacLFY 基因不仅在生殖器官中表达,而且在营养器官中表达。此外,这种表达模式与在烟草中由 PlacLFY 的潜在启动子区域控制的 GUS 报告基因的表达模式一致。