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Published on February 13, 2003; 10.1104/pp.102.016071


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Received October 10, 2002
Returned for revision November 24, 2002
Accepted December 17, 2002

The Sym35 Gene Required for Root Nodule Development in Pea Is an Ortholog of Nin from Lotus japonicus

Alexey Y. Borisov , Lene H. Madsen , Viktor E. Tsyganov , Yosuke Umehara , Vera A. Voroshilova , Arsen O. Batagov , Niels Sandal , Anita Mortensen , Leif Schauser , Noel Ellis , Igor A. Tikhonovich , and Jens Stougaard *

All-Russia Research Institute for Agricultural Microbiology, St. Petersburg, Pushkin 8, Podbelsky Chaussee, 3, 196608, Russia (A.Y.B., V.E.T., V.A.V., A.O.B., I.A.T.); Department of Molecular Biology, Laboratory of Gene Expression, University of Aarhus, Gustav Wieds Vej 10, DK-8000, Aarhus C, Denmark (L.H.M., Y.U., N.S., A.M., L.S., J.S.); and John Innes Centre, Norwich NR4 7UH, United Kingdom (N.E.)

* Corresponding author; email: stougaard{at}mbio.aau.dk.

Comparative phenotypic analysis of pea (Pisum sativum) sym35 mutants and Lotus japonicus nin mutants suggested a similar function for the PsSym35 and LjNin genes in early stages of root nodule formation. Both the pea and L. japonicus mutants are non-nodulating but normal in their arbuscular mycorrhizal association. Both are characterized by excessive root hair curling in response to the bacterial microsymbiont, lack of infection thread initiation, and absence of cortical cell divisions. To investigate the molecular basis for the similarity, we cloned and sequenced the PsNin gene, taking advantage of sequence information from the previously cloned LjNin gene. An RFLP analysis on recombinant inbred lines mapped PsNin to the same chromosome arm as the PsSym35 locus and direct evidence demonstrating that PsNin is the PsSym35 gene was subsequently obtained by cosegregation analysis and sequencing of three independent Pssym35 mutant alleles. L. japonicus and pea root nodules develop through different organogenic pathways, so it was of interest to compare the expression of the two orthologous genes during nodule formation. Overall, a similar developmental regulation of the PsNin and LjNin genes was shown by the transcriptional activation in root nodules of L. japonicus and pea. In the indeterminate pea nodules, PsNin is highly expressed in the meristematic cells of zone I and in the cells of infection zone II, corroborating expression of LjNin in determinate nodule primordia. At the protein level, seven domains, including the putative DNA binding/dimerization RWP-RK motif and the PB1 heterodimerization domain, are conserved between the LjNIN and PsNIN proteins.




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