Ref ID: 18495
Author:
Oier Etxebeste,
Aitor Garzia,
Erika Herrero-García,
Marc S. Cortese,
Eduardo A. Espeso,
Unai Ugalde
Author address:
Department of Applied Chemistry, Faculty of Chemistry, University of The Basque Country, Manuel de Lardizabal
3, 20018, San Sebastian, Spain. Â
2.
Dept. Medicina Molecular y Celular, Centro de Investigaciones Biológicas (CSIC),
Ramiro de Maeztu,
Full conference title:
11 th European Conference on Fungal Genetics
Abstract:
The early stages of asexual development in the model fungus Aspergillus nidulans are controlled at the molecular
level by a discrete number of regulatory proteins that includes the bZIP8208;type transcription factor (TF) FlbB.
Vegetative hyphae contain two main pools of FlbB, one at the tip and the other at the most apical nucleus. The
apical pool requires the interaction with the positional regulator FlbE at or in the proximity of the Spitzenkörper.
This interaction requires in FlbB a functional bZIP domain, specific central regions and a highly conserved Cys
residue. Nuclear FlbB is renewed after each mitotic cycle and under appropriate conditions, activates the cMyb8208;
type TF FlbD. Both factors, in turn, jointly activate the expression of the conidiation8208;specific TF brlA.
A 2D8208;PAGE screening of proteins in wild type and 8710;flbB strains showed that the concentration of specific stress8208;
response proteins was controlled through FlbB. gmcA, a previously uncharacterized glucose8208;methanol8208;choline
oxidoreductase coding gene, shows miss8208;scheduled expression in a 916;flbB genetic background and the derived
protein is required during development under alkaline pH conditions. Sequencing of mRNA from both vegetative
and asexual samples provides for a wide overview on the genes and pathways under the hypothetic transcriptional
control of FlbB activity. Preliminary results obtained in the functional characterization of some of these genes are
also presented.
Overall, the functional versatility of FlbB provides for a new outlook on morphogenetic change and focuses our
future work on the study of the molecular mechanisms through which this TF regulates different cellular processes
during development.
Abstract Number: PR7.2
Conference Year: 2012
Link to conference website: http://www.ecfg.info/images/Abstract_Book_Electronic.pdf
New link: NULL
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