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在百脉根的T-DNA转化后鉴定出的缺乏根瘤形成的共生突变体。

Symbiotic mutants deficient in nodule establishment identified after T-DNA transformation of Lotus japonicus.

作者信息

Schauser L, Handberg K, Sandal N, Stiller J, Thykjaer T, Pajuelo E, Nielsen A, Stougaard J

机构信息

Department of Molecular and Structural Biology, University of Aarhus, Denmark.

出版信息

Mol Gen Genet. 1998 Sep;259(4):414-23. doi: 10.1007/s004380050831.

Abstract

Nitrogen-fixing root nodules develop on legumes as a result of an interaction between host plants and soil bacteria collectively referred to as rhizobia. The organogenic process resulting in nodule development is triggered by the bacterial microsymbiont, but genetically controlled by the host plant genome. Using T-DNA insertion as a tool to identify novel plant genes that regulate nodule ontogeny, we have identified two putatively tagged symbiotic loci, Ljsym8 and Ljsym13, in the diploid legume Lotus japonicus. The sym8 mutants are arrested during infection by the bacteria early in the developmental process. The sym13 mutants are arrested in the final stages of infection, and ineffective nodules are formed. These two plant mutant lines were identified in progeny from 1112 primary transformants obtained after Agrobacterium tumefaciens T-DNA-mediated transformation of L. japonicus and subsequent screening for defects in the symbiosis with Mesorhizobium loti. Additional nontagged mutants arrested at different developmental stages were also identified and genetic complementation tests assigned all the mutations to 16 monogenic symbiotic loci segregating recessive mutant alleles. In the screen reported here independent symbiotic loci thus appeared with a frequency of approximately 1.5%, suggesting that a relatively large set of genes is required for the symbiotic interaction.

摘要

固氮根瘤在豆科植物上形成,这是宿主植物与统称为根瘤菌的土壤细菌之间相互作用的结果。导致根瘤发育的器官发生过程由细菌微共生体触发,但由宿主植物基因组进行遗传控制。利用T-DNA插入作为一种工具来鉴定调控根瘤个体发育的新植物基因,我们在二倍体豆科植物百脉根中鉴定出了两个推定被标签标记的共生位点Ljsym8和Ljsym13。sym8突变体在发育过程早期被细菌感染时就停滞了。sym13突变体在感染的最后阶段停滞,并形成无效根瘤。这两个植物突变体系是在通过根癌农杆菌T-DNA介导转化百脉根并随后筛选与中慢生根瘤菌共生缺陷后获得的1112个初级转化体的后代中鉴定出来的。还鉴定出了在不同发育阶段停滞的其他未被标签标记的突变体,遗传互补试验将所有突变分配到16个单基因共生位点,这些位点分离出隐性突变等位基因。在本文报道的筛选中,独立的共生位点出现频率约为1.5%,这表明共生相互作用需要相对大量的基因。

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