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The Arabidopsis bHLH25 and bHLH27 transcription factors contribute to susceptibility to the cyst nematode Heterodera schachtii
Author(s) -
Jin Jing,
Hewezi Tarek,
Baum Thomas J.
Publication year - 2011
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/j.1365-313x.2010.04424.x
Subject(s) - heterodera schachtii , biology , arabidopsis , complementation , microbiology and biotechnology , soybean cyst nematode , gene , pathosystem , genetics , transcription factor , transcription (linguistics) , nematode , mutant , ecology , linguistics , philosophy
Summary Successful cyst nematode parasitism depends on the formation and maintenance of feeding sites (syncytia) in host roots, and these processes are highly regulated by the interaction between the cyst nematode and the host. Using an integrated research approach and the Arabidopsis– Beta vulgaris (sugar beet) cyst nematode ( Heterodera schachtii ) pathosystem, we have determined that the two Arabidopsis basic helix–loop–helix transcription factors bHLH25 and bHLH27 positively influence cyst nematode parasitism. Promoter studies indicated that as early as 1 day post‐inoculation, both transcription factor genes were upregulated in developing syncytia, whereas in non‐infected plants, these two promoters were not found to be active in the same cells. By using yeast two‐hybrid analyses and bimolecular fluorescence complementation assays, we documented that the two bHLH transcription factors can dimerize in planta . Transgenic Arabidopsis plants overexpressing either one or both of the bHLH genes exhibited altered morphology of roots and shoots, as well as an increased susceptibility to H. schachtii . bhlh25 or bhlh27 single mutants were without strong phenotypes, presumably because of functional redundancies in this gene family. However, the bhlh25 bhlh27 double mutant was less susceptible to H. schachtii , confirming an important conducive role of the co‐expression of both transcription factor genes for cyst nematode parasitism. Our results document an example of pathogen‐induced ectopic co‐expression of two regulatory genes to enhance pathogen success, although these transcription factors apparently do not function in concert in non‐infected plants. This is an intriguing biological phenomenon that highlights the complexity of obligate biotrophic plant–pathogen interactions, like those of cyst nematodes.