Csanádi G, Szécsi J, Kaló P, Kiss P, Endre G, Kondorosi A, Kondorosi E, Kiss G B
Institute of Genetics, Biological Research Center, Hungarian Academy of Sciences, Szeged, Hungary.
Plant Cell. 1994 Feb;6(2):201-13. doi: 10.1105/tpc.6.2.201.
To demonstrate the importance of an extensively studied early nodulin gene ENOD12 in symbiotic nodule development, plants of different Medicago sativa subspecies were tested for the presence or absence of ENOD12 alleles. In M. s. ssp coerulea w2 (Mcw2), two ENOD12 genes were detected, whereas in M. s. ssp quasifalcata k93 (Mqk93) only one gene was present. In both plants, the ENOD12 genes were expressed in nodules induced by Rhizobium meliloti. The nucleotide sequence of the ENOD12 genes showed that the two Mcw2-specific genes were similar to the ENOD12A and ENOD12B genes of the tetraploid M. s. ssp sativa. ENOD12 from Mqk93 was similar to the corresponding gene found in M. truncatula. From the aligned ENOD12 sequences, an evolutionary tree was constructed. Genetic analysis of the progenies of a cross between Mqk93 and Mcw2 showed that several offspring in F1 carried a null allele originating from Mcw2, and among the F2 progenies, plants with the null allele only lacking the ENOD12 gene appeared. Surprisingly, the ENOD12-deficient plants were similar to their wild-type parents in viability, nodule development, nodule structure, and nitrogen fixation efficiency. Therefore, we concluded that in Medicago the ENOD12 gene is not required for symbiotic nitrogen fixation. Furthermore, we proposed that the heterozygous nature of these legumes can be exploited for the identification of mutated alleles of other known nodulin genes; this will permit the construction of plant mutants deficient in these genes.
为了证明广泛研究的早期结瘤素基因ENOD12在共生结瘤发育中的重要性,对不同紫花苜蓿亚种的植株进行了ENOD12等位基因存在与否的检测。在紫花苜蓿ssp coerulea w2(Mcw2)中,检测到两个ENOD12基因,而在紫花苜蓿ssp quasifalcata k93(Mqk93)中仅存在一个基因。在这两种植株中,ENOD12基因均在苜蓿根瘤菌诱导形成的根瘤中表达。ENOD12基因的核苷酸序列表明,两个Mcw2特有的基因与四倍体紫花苜蓿ssp sativa的ENOD12A和ENOD12B基因相似。Mqk93中的ENOD12与蒺藜苜蓿中发现的相应基因相似。根据比对的ENOD12序列构建了进化树。对Mqk93和Mcw2杂交后代的遗传分析表明,F1代中的几个后代携带了一个源自Mcw2的无效等位基因,在F2代后代中,出现了仅缺失ENOD12基因的无效等位基因植株。令人惊讶的是,ENOD12缺陷型植株在活力、根瘤发育、根瘤结构和固氮效率方面与其野生型亲本相似。因此,我们得出结论,在苜蓿中,共生固氮不需要ENOD12基因。此外,我们提出,可以利用这些豆科植物的杂合特性来鉴定其他已知结瘤素基因的突变等位基因;这将有助于构建这些基因缺陷的植物突变体。