Two double mutants carrying pea symbiotic gene pairs sym13, sym40 and sym33, sym40, respectively, were constructed using single mutants blocked at different nodule developmental stages: E135f (sym13), SGEFix–‑1 (sym40) and SGEFix–‑2 (sym33). The epistasis of the mutant allele sym40 over the mutant allele sym13 and sym33 over sym40 was shown with respect to nodule histological and ultrastructural organisation. Thus, the proposed earlier sequential functioning of genes during infection process: Sym33→Sym40→Sym13 has been confirmed
International audienceThe Pisum sativum L. mutant RisNod24 (Pssym36) is defective for arbuscular myc...
In this study a supernodulating non-fixing (AR−) pea mutant FN1 was compared with the supernodulatin...
In wild pea varieties two genes, sym1 and sym2, have been identified that cause resistance to Europe...
Using pea single mutant lines SGEFix–-2 (sym33) and RisFixV (sym42), which are characterized by diff...
The studies on symbiotic nitrogen fixation between pea (Pisum sativum L.) and Rhizobium leguminosaru...
In legumes, perception of rhizobial lipochitooligosacharide-based molecules (Nod factors) and subseq...
Eight symbiotic mutants of pea (Pisum sativum L.) induced by chemical mutagenesis have been studied ...
Eleven pea mutants, displaying a greatly reduced number of root nodules or lacking such nodules comp...
Endosymbiotic interactions form a fundament of life as we know it and are characterized by the form...
Rhizobium leguminosarum bv. viciae, which nodulates pea and vetch, makes a mixture of secreted nodul...
In pea (Pisum sativum) up to 50 nodulation mutants are known, several of which are affected in the e...
The symbiotic interaction between Rhizobium bacteria and leguminous plants results in the formation ...
Thirteen stable nonnodulating mutant lines of pea (Pisum sativum L.) originating from cv. Finale wer...
Genetic and molecular mechanisms of development are compared for two major plant}microbe endosymbios...
Large collections of pea symbiotic mutants were accumulated in the 1990s, but the causal genes for a...
International audienceThe Pisum sativum L. mutant RisNod24 (Pssym36) is defective for arbuscular myc...
In this study a supernodulating non-fixing (AR−) pea mutant FN1 was compared with the supernodulatin...
In wild pea varieties two genes, sym1 and sym2, have been identified that cause resistance to Europe...
Using pea single mutant lines SGEFix–-2 (sym33) and RisFixV (sym42), which are characterized by diff...
The studies on symbiotic nitrogen fixation between pea (Pisum sativum L.) and Rhizobium leguminosaru...
In legumes, perception of rhizobial lipochitooligosacharide-based molecules (Nod factors) and subseq...
Eight symbiotic mutants of pea (Pisum sativum L.) induced by chemical mutagenesis have been studied ...
Eleven pea mutants, displaying a greatly reduced number of root nodules or lacking such nodules comp...
Endosymbiotic interactions form a fundament of life as we know it and are characterized by the form...
Rhizobium leguminosarum bv. viciae, which nodulates pea and vetch, makes a mixture of secreted nodul...
In pea (Pisum sativum) up to 50 nodulation mutants are known, several of which are affected in the e...
The symbiotic interaction between Rhizobium bacteria and leguminous plants results in the formation ...
Thirteen stable nonnodulating mutant lines of pea (Pisum sativum L.) originating from cv. Finale wer...
Genetic and molecular mechanisms of development are compared for two major plant}microbe endosymbios...
Large collections of pea symbiotic mutants were accumulated in the 1990s, but the causal genes for a...
International audienceThe Pisum sativum L. mutant RisNod24 (Pssym36) is defective for arbuscular myc...
In this study a supernodulating non-fixing (AR−) pea mutant FN1 was compared with the supernodulatin...
In wild pea varieties two genes, sym1 and sym2, have been identified that cause resistance to Europe...