Agriculture Reference
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sativum (pea), and MtLYK3 / MtLYK4 and MtNFP in Medicago truncatula ,
respectively (Indrasumunar 2007; Indrasumunar et al . 2010).
Unlike the NFR genes identified in the other legume species, both NFR1
and NFR5 genes in soybean are duplicated, resulting in GmNFR1ʱ/GmNFR1β
and GmNFR5ʱ/GmNFR5β . The duplicated copies of GmNFR5 are slightly
more conserved than the duplicated copies of GmNFR1 , at both the nucleotide
and protein sequence level (Table 1). In regards to extracellular and
transmembrane domains, the duplicated copies of GmNFR5 are also more
similar than the GmNFR1 duplicated copies. However, the kinase domain of
both GmNFR1 and GmNFR5 duplicated copies are equally similar (Table 1).
GmNFR1ʱ and β appear to have slightly different functions, where GmNFR1ʱ
has a higher affinity for Nod factor than GmNFR1β . In contrast, GmNFR5ʱ
and β , which share a high degree of similarity, appear to complement one
another (Indrasumunar 2007; Indrasumunar et al . 2010).
Table 1. Similarity between duplicated gene copies of GmNFR1 and
GmNFR5
Nucleotides
level
Protein
level
Extra
cellular
Trans
Membrane
Kinase
Domain
GmNFR1ʱ
and
GmNFR1β
94%
90%
82%
74%
96%
GmNFR5ʱ
and
GmNFR5β
95%
93%
91%
96%
96%
GmNFR1ʱ and GmNFR5ʱ/β are required for the earliest physiological and
cellular responses to Nod factors. As has been reported for Nod factor receptor
genes of other legume species, GmNFR1 and GmNFR5 are required for root
hair swelling and curling. They are also required for downstream nodulation
signaling events, such as the induced expression of critical nodulation genes.
Mutations in any of GmNFR1ʱ or GmNFR5ʱ/β result in plants that either do
not respond, or show an attenuated response, to B. japonicum inoculation
(Indrasumunar 2007; Indrasumunar et al . 2010).
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