Bonhomme S, Horlow C, Vezon D, de Laissardière S, Guyon A, Férault M, Marchand M, Bechtold N, Pelletier G
INRA Station de Génétique et d'Amélioration des Plantes, Centre de Versailles-Grignon, Versailles, France.
Mol Gen Genet. 1998 Dec;260(5):444-52. doi: 10.1007/s004380050915.
Many genes are thought to be expressed during the haploid phase in plants, however, very few haploid-specific genes have been isolated so far. T-DNA insertion mutagenesis is a powerful tool for generating mutations that affect gametophyte viability and function, as disruption of a gene essential for these processes should lead to a defect in the transmission of the gametes. Mutants can therefore be screened on the basis of segregation distortion for a reporter resistance gene contained in the T-DNA. We have screened the Versailles collection of Arabidopsis transformants for 1:1 KanR:KanS segregation after selfing, focussing on gametophyte mutations which show normal transmission through one gametophyte and cause lethality or dysfunction of the other. Only 1.3% (207) of the 16,000 lines screened were scored as good candidates. Thorough genetic analysis of 38 putative T-DNA transmission defect lines (Ttd) identified 8 defective gametophyte mutants, which all showed 0 to 1% T-DNA transmission through the pollen. During the screen, we observed a high background of low-penetrance mutations, often affecting the function of both gametophytes, and many lines which were likely to carry chromosomal rearrangements. The reasons for the small number of retained lines (all male gametophytic) are discussed, as well as the finding that, for most of them, residual T-DNA transmission is obtained through the affected gametophyte.
许多基因被认为在植物的单倍体阶段表达,然而,到目前为止,很少有单倍体特异性基因被分离出来。T-DNA插入诱变是一种产生影响配子体活力和功能的突变的有力工具,因为这些过程所必需的基因的破坏应该导致配子传递的缺陷。因此,可以基于T-DNA中包含的报告抗性基因的分离畸变来筛选突变体。我们已经筛选了拟南芥转化体的凡尔赛收集品系,以检测自交后1:1的卡那霉素抗性(KanR):卡那霉素敏感(KanS)分离情况,重点关注配子体突变,这些突变通过一个配子体显示正常传递,并导致另一个配子体致死或功能障碍。在筛选的16000个品系中,只有1.3%(207个)被评为良好候选品系。对38个推定的T-DNA传递缺陷系(Ttd)进行的全面遗传分析鉴定出8个有缺陷的配子体突变体,它们通过花粉的T-DNA传递率均为0%至1%。在筛选过程中,我们观察到低 penetrance 突变的高背景,这些突变通常影响两个配子体的功能,以及许多可能携带染色体重排的品系。讨论了保留品系数量少(均为雄配子体)的原因,以及对其中大多数品系而言,通过受影响的配子体获得残余T-DNA传递的发现。