4.7 Article

Inactivation of Duplicated Nod Factor Receptor 5 (NFR5) Genes in Recessive Loss-of-Function Non-Nodulation Mutants of Allotetraploid Soybean (Glycine max L. Merr.)

Journal

PLANT AND CELL PHYSIOLOGY
Volume 51, Issue 2, Pages 201-214

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/pcp/pcp178

Keywords

Gene duplication; Glycine max; GmNFR5; Nodulation; Retroelement; Symbiosis

Funding

  1. Australian Research Council [CEO34821]
  2. Queensland State Government
  3. University of Queensland Strategic Fund
  4. AusAID
  5. Sugar Research and Development Corporation (SRDC)

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Chemically induced non-nodulating nod139 and nn5 mutants of soybean (Glycine max) show no visible symptoms in response to rhizobial inoculation. Both exhibit recessive Mendelian inheritance suggesting loss of function. By allele determination and genetic complementation in nod139 and nn5, two highly related lipo-oligochitin LysM-type receptor kinase genes in Glycine max were cloned; they are presumed to be the critical nodulation-inducing (Nod) factor receptor similar to those of Lotus japonicus, pea and Medicago truncatula. These duplicated receptor genes were called GmNFR5 alpha and GmNFR5 beta. Nonsense mutations in GmNFR5 alpha and GmNFR5 beta were genetically complemented by both wild-type GmNFR5 alpha and GmNFR5 beta in transgenic roots, indicating that both genes are functional. Both genes lack introns. In cultivar Williams82 GmNFR5 alpha is located in chromosome 11 and in tandem with GmLYK7 (a related LysM receptor kinase gene), while GmNFR5 beta is in tandem with GmLYK4 in homologous chromosome 1, suggesting ancient synteny and regional segmental duplication. Both genes are wild type in G. soja CPI100070 and Harosoy63; however, a non-functional NFR5 beta allele (NFR5 beta*) was discovered in parental lines Bragg and Williams, which harbored an identical 1,407bp retroelement-type insertion. This retroelement (GmRE-1) and related sequences are located in several soybean genome positions. Paradoxically, putatively unrelated soybean cultivars shared the same insertion, suggesting a smaller than anticipated genetic base in this crop. GmNFR5 alpha but not GmNFR5 beta* was expressed in inoculated and uninoculated tap and lateral root portions at about 10-25% of GmATS1 (ATP synthase subunit 1), but not in trifoliate leaves and shoot tips.

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