Proceedings of the XLVII Italian
Society of Agricultural Genetics - SIGA Annual Congress
Verona,
Italy - 24/27 September, 2003
ISBN 88-900622-4-X
Poster
Abstract - 4.06
DISSECTING
GRAPE LEAF DEVELOPMENT AND SENESCENCE AT THE MOLECULAR LEVEL
C. MOSER*, M.
PINDO*, C. SEGALA*, P. FONTANA*, E. BLANZIERI**, P. GATTO*, A. ZAMBONI*, M.
BERTAMINI*+, N. NEDUCHENZIAN*+, R. VELASCO*
*) Istituto
Agrario S. Michele a/Adige; S. Michele a/Adige-Trento (+Area
Biologia Avanzata; Unità Operativa Viticoltura)
**) Dip. di
Informatica e Telecomunicazioni Università di Trento
grape, gene
expression, ESTs, arrays, leaf development
Leaf development
and senescence are biological processes under tight genetic control. It has
been observed that during leaf expansion photosynthetic rates typically
increase and vice-versa during leaf senescence they decline. A
photosynthetically efficient leaf is important during ripening of grape berries
in order to achieve high sugar and secondary metabolites concentrations.
High-throughput sequencing of ESTs and gene expression analysis, on a
genome-wide scale, have opened new possibilities to shed light on complex
biological questions like leaf senescence.
Following such an
approach we have started two years ago the construction and characterization of
cDNA libraries from different grape tissues and the collection of a large number of expressed sequences. The
sequence information has been processed via bioinformatics tools in order to
estimate redundancy and to assign a putative function to each clone on homology
base. Up to now we sequenced about
8000 ESTs organized in a searchable and soon publicly accessible grapevine
database. Clustering of the sequences revealed that about 70 - 85 % of them,
are found only in one tissue, suggesting a marked organ specialization, at
least for the highly abundant transcripts. A subset of the cDNA clones (ca.
2300 unigenes) have been spotted on high-density nylon filters and probed with
RNA isolated from cv. 'Pinot noir'
leaves in 5 different developmental stages. Analysis of gene expression data has been carried out by
looking at genes involved in specific metabolic functions and by clustering
methods. In addition, transcription profiles have been interpreted in the light
of physiological measurements like pigments changes, electron transport
activities and total soluble proteins content.
Preliminary
results, to be validated and further characterized, identified a group of genes
that are up-regulated during leaf senescence.