September
1998
, Volume
11
, Number
9
Pages
915
-
923
Authors
Preeti
Dahiya
,
D. Janine
Sherrier
,
Igor V.
Kardailsky
,
Alexey Y.
Borisov
,
and
Nicholas J.
Brewin
Affiliations
John Innes Centre, Colney Lane, Norwich, NR4 7UH, Great Britain
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RelatedArticle
Accepted 12 May 1998.
Abstract
The distribution of a lectinlike glycoprotein, PsNLEC-1, was examined with a specific antiserum in nodule tissue from a symbiotically defective pea mutant, Sprint2Fix¯(sym31), and the parent line, Sprint2. Immunostaining of Western blots (immunoblots) revealed that, whereas wild-type nodules contained three antigenic isoforms of PsNLEC-1, nodule homogenates of mutant sym31 contained only one isoform, PsNLEC-1C. Fractionation studies indicated that PsNLEC-1C was not associated with symbiosomes in either the mutant or the wild-type parent (unlike the other two isoforms from wild-type nodules). Light microscopy revealed that PsNLEC-1 antigen was more abundant in the infected tissues of wild-type nodules than in nodules of sym31. By contrast, in situ hybridization indicated that the PsNlec1 gene transcript was strongly expressed in infected cells of both Sprint2 and sym31 nodule tissues. At the ultrastructural level, most of the PsNLEC-1 antigen in sym31 nodule tissue was visualized as inclusion bodies in the vacuolar compartment of infected host cells but it was apparently absent from the symbiosome compartment. The results suggest an aberrant vesicle targeting pathway during symbiosome development in this mutant.
JnArticleKeywords
Additional keywords:
Golgi body,
lectin,
legume,
nitrogen fixation,
Pisum sativum,
Rhizobium leguminosarum bv. viciae.
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ArticleCopyright
© 1998 The American Phytopathological Society