van der Graaff E, Nussbaumer C, Keller B
Institute of Plant Biology, University of Zürich, Zollikerstrasse 107, 8008 Zürich, Switzerland.
Mol Genet Genomics. 2003 Nov;270(3):243-52. doi: 10.1007/s00438-003-0901-8. Epub 2003 Aug 9.
Activation tagging of the gene LEAFY PETIOLE (LEP) with a T-DNA construct induces ectopic leaf blade formation in Arabidopsis, which results in a leafy petiole phenotype. In addition, the number of rosette leaves produced prior to the onset of bolting is reduced, and the rate of leaf initiation is retarded by the activation tagged LEP gene. The ectopic leaf blade results from an invasion of the petiole region by the wild-type leaf blade. In order to isolate mutants that are specifically disturbed in the outgrowth of the leaf blade, second site mutagenesis was performed using ethane methanesulphonate (EMS) on a transgenic line that harbours the activation-tagged LEP gene and exhibits the leafy petiole phenotype. A collection of revertant for leafy petiole (rlp lines was isolated that form petiolated rosette leaves in the presence of the activated LEP gene, and could be classified into three groups. The class III rlp lines also display altered leaf development in a wild-type (non-transgenic) background, and are probably mutated in genes that affect shoot or leaf development. The rlp lines of classes I and II, which represent the majority of revertants, do not affect leaf blade outgrowth in a wild-type (non-transgenic) background. This indicates that LEP regulates a subset of the genes involved in the process of leaf blade outgrowth, and that genetic and/or functional redundancy in this process compensates for the loss of RLP function during the formation of the wild-type leaf blade. More detailed genetic and morphological analyses were performed on a selection of the rlp lines. Of these, the dominant rlp lines display complete reversion of (1) the leafy petiole phenotype, (2) the reduction in the number of rosette leaves and (3) the slower leaf initiation rate caused by the activation-tagged LEP gene. Therefore, these lines are potentially mutated in genes for interacting partners of LEP or in downstream regulatory genes. In contrast, the recessive rlp lines exhibit a specific reversion of the leafy petiole phenotype. Thus, these lines are most probably mutated in genes specific for the outgrowth of the leaf blade. Further functional analysis of the rlp mutations will contribute to the dissection of the complex pathways underlying leaf blade outgrowth.
用T-DNA构建体对LEAFY PETIOLE(LEP)基因进行激活标签标记,可在拟南芥中诱导异位叶片形成,从而导致叶状叶柄表型。此外,抽薹开始前产生的莲座叶数量减少,并且激活标签标记的LEP基因会延缓叶片起始速率。异位叶片是由野生型叶片侵入叶柄区域导致的。为了分离在叶片生长过程中受到特异性干扰的突变体,使用乙烷甲磺酸盐(EMS)对携带激活标签标记的LEP基因并表现出叶状叶柄表型的转基因品系进行了二次位点诱变。分离出了一组叶状叶柄回复突变体(rlp品系),它们在激活的LEP基因存在的情况下形成具叶柄的莲座叶,并且可分为三组。III类rlp品系在野生型(非转基因)背景下也表现出叶片发育改变,可能是影响茎或叶发育的基因突变所致。代表大多数回复突变体的I类和II类rlp品系在野生型(非转基因)背景下不影响叶片生长。这表明LEP调节参与叶片生长过程的一部分基因,并且该过程中的遗传和/或功能冗余在野生型叶片形成过程中补偿了RLP功能的丧失。对一些rlp品系进行了更详细的遗传和形态学分析。其中,显性rlp品系表现出(1)叶状叶柄表型、(2)莲座叶数量减少和(3)激活标签标记的LEP基因导致的叶片起始速率减慢的完全回复。因此,这些品系可能在LEP相互作用伙伴的基因或下游调控基因中发生了突变。相比之下,隐性rlp品系表现出叶状叶柄表型的特异性回复。因此,这些品系很可能是在叶片生长特有的基因中发生了突变。对rlp突变的进一步功能分析将有助于剖析叶片生长背后的复杂途径。