PAG-IV Plant Genome IV Conference

Town & Country Conference Center, San Diego, CA, January, 1995.


P3
Isolation and Characterization of Drought-Stress Associated cDNAs from Zea mays

MICHAEL U. HOEFER and PETER WESTHOFF
Heinrich-Heine-University, Dept. of Botany, Universitaetsstrasse 1, D-40225 Duesseldorf, Germany

Progressive water deficit alterations are known to change the expression of many genes in plants. Recent research has focussed primarily on dessication-induced genes like the lea-genes which have been characterized in detail. However the large variability of drought response in species and particulary variety-specific tolerances or adaptions are hardly understood at the molecular level. Drought tolerance is supposed to be a polygenic trait. It is expected that the differences in the expression levels of drought-stress associated genes are partially responsible for quantitative variations of drought response traits. These cDNAs may be regarded as "candidate" genes contributing to drought-tolerance and could therefore be used for QTL analysis. We have started with the isolation of a comprehensive set of cDNAs whose mRNAs show altered expression as a result of water deficit gradients which range from a moderate to severe drought-stress in young maize plants. To date differential screening of a leaf cDNA library yielded about 15 putative drought-stress related cDNAs which have been characterized by sequencing and with northern hybridization techniques. The identified cDNAs belong to the highly abundant hsp70s, ubiquitines, proline-rich and phospholipid transfer proteins, alpha-tubulines, lipoxygenases, "seed imbibition" protein and ABA/fruit ripening homologue proteins. Five to ten times more of the corresponding mRNAs for the majority of these cDNAs accumulate preferentially in green leaves under conditions of moderate drought-stress when compared with normal plants. A few cDNAs are selectively induced under conditions of more severe drought-stress. For a more complete investigation of drought associated cDNAs, including those with lower abundance, shoot- and root-cDNA libraries are presently screened by subtractive hybridization techniques.
(This investigation is part of Network B3 of the PTP project supported by the European Union)


Return to Previous Page or Intl-PAG Homepage