Zhao Yinhe, Wang Guoying, Zhang Jinpeng, Yang Junbo, Peng Shang, Gao Lianming, Li Chengyun, Hu Jinyong, Li Dezhu, Gao Lizhi
Laboratory of Biodiversity and Plant Biogeography, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650204, China.
Ann Bot. 2006 Jul;98(1):157-63. doi: 10.1093/aob/mcl081. Epub 2006 May 4.
Asarum caudigerum (Aristolochiaceae) is an important species of paleoherb in relation to understanding the origin and evolution of angiosperm flowers, due to its basal position in the angiosperms. The aim of this study was to isolate floral-related genes from A. caudigerum, and to infer evolutionary relationships among florally expression-related genes, to further illustrate the origin and diversification of flowers in angiosperms.
A subtracted floral cDNA library was constructed from floral buds using suppression subtractive hybridization (SSH). The cDNA of floral buds and leaves at the seedling stage were used as a tester and a driver, respectively. To further identify the function of putative MADS-box transcription factors, phylogenetic trees were reconstructed in order to infer evolutionary relationships within the MADS-box gene family.
In the forward-subtracted floral cDNA library, 1920 clones were randomly sequenced, from which 567 unique expressed sequence tags (ESTs) were obtained. Among them, 127 genes failed to show significant similarity to any published sequences in GenBank and thus are putatively novel genes.
Phylogenetic analysis indicated that a total of 29 MADS-box transcription factors were members of the APETALA3(AP3) subfamily, while nine others were putative MADS-box transcription factors that formed a cluster with MADS-box genes isolated from Amborella, the basal-most angiosperm, and those from the gymnosperms. This suggests that the origin of A. caudigerum is intermediate between the angiosperms and gymnosperms.
尾花细辛(马兜铃科)是一种重要的古草本植物,因其在被子植物中的基部位置,对于理解被子植物花的起源与演化具有重要意义。本研究旨在从尾花细辛中分离与花相关的基因,并推断花表达相关基因之间的进化关系,以进一步阐明被子植物花的起源与多样化。
利用抑制性消减杂交(SSH)技术,从花芽构建消减花cDNA文库。分别以苗期花芽和叶片的cDNA作为试验方和驱动方。为进一步鉴定假定的MADS盒转录因子的功能,构建系统发育树以推断MADS盒基因家族内部的进化关系。
在正向消减花cDNA文库中,随机测序1920个克隆,获得567个独特的表达序列标签(EST)。其中,127个基因与GenBank中任何已发表序列均无显著相似性,因此被认为是新基因。
系统发育分析表明,共有29个MADS盒转录因子属于APETALA3(AP3)亚家族,另外9个是假定的MADS盒转录因子,它们与从最基部的被子植物无油樟以及裸子植物中分离出的MADS盒基因形成一个聚类。这表明尾花细辛的起源介于被子植物和裸子植物之间。