Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development

<p>Abstract</p> <p>Background</p> <p>The Arabidopsis <it>SEUSS </it>(<it>SEU</it>) gene encodes a transcriptional adaptor protein that is required for a diverse set of developmental events, including floral organ identity specification, as well a...

Full description

Bibliographic Details
Main Authors: Nole-Wilson Staci, Rueschhoff Elizabeth E, Bhatti Huda, Franks Robert G
Format: Article
Language:English
Published: BMC 2010-09-01
Series:BMC Plant Biology
Online Access:http://www.biomedcentral.com/1471-2229/10/198
_version_ 1811266348913786880
author Nole-Wilson Staci
Rueschhoff Elizabeth E
Bhatti Huda
Franks Robert G
author_facet Nole-Wilson Staci
Rueschhoff Elizabeth E
Bhatti Huda
Franks Robert G
author_sort Nole-Wilson Staci
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The Arabidopsis <it>SEUSS </it>(<it>SEU</it>) gene encodes a transcriptional adaptor protein that is required for a diverse set of developmental events, including floral organ identity specification, as well as gynoecium, ovule and embryo development. In order to better understand the molecular mechanisms of <it>SEUSS </it>action we undertook a genetic modifier screen to identify <it>seuss-modifier </it>(<it>sum</it>) mutations.</p> <p>Results</p> <p>Screening of M2 lines representing approximately 5,000 M1 individuals identified mutations that enhance the <it>seuss </it>mutant phenotypic disruptions in ovules and gynoecia; here we describe the phenotype of the <it>sum63 </it>mutant and enhanced disruptions of ovule and gynoecial development in the <it>seu sum63 </it>double mutant. Mapping and genetic complementation tests indicate that <it>sum63 </it>is allelic to <it>CYP85A2 </it>(AT3G30180) a cytochrome p450 enzyme that catalyzes the final steps in the synthesis of the phytohormone brassinolide.</p> <p>Conclusions</p> <p>Our identification of mutations in <it>CYP85A2 </it>as enhancers of the <it>seuss </it>mutant phenotype suggests a previously unrecognized role for brassinolide synthesis in gynoecial and ovule outer integument development. The work also suggests that <it>seuss </it>mutants may be more sensitive to the loss or reduction of brassinolide synthesis than are wild type plants.</p>
first_indexed 2024-04-12T20:40:21Z
format Article
id doaj.art-476154b437fb4269a358aa2165212db7
institution Directory Open Access Journal
issn 1471-2229
language English
last_indexed 2024-04-12T20:40:21Z
publishDate 2010-09-01
publisher BMC
record_format Article
series BMC Plant Biology
spelling doaj.art-476154b437fb4269a358aa2165212db72022-12-22T03:17:25ZengBMCBMC Plant Biology1471-22292010-09-0110119810.1186/1471-2229-10-198Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule developmentNole-Wilson StaciRueschhoff Elizabeth EBhatti HudaFranks Robert G<p>Abstract</p> <p>Background</p> <p>The Arabidopsis <it>SEUSS </it>(<it>SEU</it>) gene encodes a transcriptional adaptor protein that is required for a diverse set of developmental events, including floral organ identity specification, as well as gynoecium, ovule and embryo development. In order to better understand the molecular mechanisms of <it>SEUSS </it>action we undertook a genetic modifier screen to identify <it>seuss-modifier </it>(<it>sum</it>) mutations.</p> <p>Results</p> <p>Screening of M2 lines representing approximately 5,000 M1 individuals identified mutations that enhance the <it>seuss </it>mutant phenotypic disruptions in ovules and gynoecia; here we describe the phenotype of the <it>sum63 </it>mutant and enhanced disruptions of ovule and gynoecial development in the <it>seu sum63 </it>double mutant. Mapping and genetic complementation tests indicate that <it>sum63 </it>is allelic to <it>CYP85A2 </it>(AT3G30180) a cytochrome p450 enzyme that catalyzes the final steps in the synthesis of the phytohormone brassinolide.</p> <p>Conclusions</p> <p>Our identification of mutations in <it>CYP85A2 </it>as enhancers of the <it>seuss </it>mutant phenotype suggests a previously unrecognized role for brassinolide synthesis in gynoecial and ovule outer integument development. The work also suggests that <it>seuss </it>mutants may be more sensitive to the loss or reduction of brassinolide synthesis than are wild type plants.</p>http://www.biomedcentral.com/1471-2229/10/198
spellingShingle Nole-Wilson Staci
Rueschhoff Elizabeth E
Bhatti Huda
Franks Robert G
Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
BMC Plant Biology
title Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
title_full Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
title_fullStr Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
title_full_unstemmed Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
title_short Synergistic disruptions in <it>seuss cyp85A2 </it>double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
title_sort synergistic disruptions in it seuss cyp85a2 it double mutants reveal a role for brassinolide synthesis during gynoecium and ovule development
url http://www.biomedcentral.com/1471-2229/10/198
work_keys_str_mv AT nolewilsonstaci synergisticdisruptionsinitseusscyp85a2itdoublemutantsrevealaroleforbrassinolidesynthesisduringgynoeciumandovuledevelopment
AT rueschhoffelizabethe synergisticdisruptionsinitseusscyp85a2itdoublemutantsrevealaroleforbrassinolidesynthesisduringgynoeciumandovuledevelopment
AT bhattihuda synergisticdisruptionsinitseusscyp85a2itdoublemutantsrevealaroleforbrassinolidesynthesisduringgynoeciumandovuledevelopment
AT franksrobertg synergisticdisruptionsinitseusscyp85a2itdoublemutantsrevealaroleforbrassinolidesynthesisduringgynoeciumandovuledevelopment