Abstract
In order to learn more about the diversity of genes expressed during flax fibre cell
wall formation, expressed sequence tags (ESTs) were obtained from a cDNA library derived
from the outer fibre-bearing tissues of flax (Linum usitatissimum) stems (cv Hermes) harvested at the mid-flowering stage. After elimination of vector
and unreadable sequences, 927 ESTs were grouped into 67 clusters and 754 singletons.
The flax ESTs have been submitted to the dbEST and GenBank databases with the accession
numbers 25939634 - 25940560 (dbEST) and CV478070 - CV478996 (GenBank). Functional
analysis allowed the grouping of ESTs into 13 functional categories and revealed that
62 % of ESTs were similar to known sequences, while 12.4 % of ESTs presented no similarity
to any known sequences and 25.6 % of ESTs corresponded to proteins of unknown function.
The most highly expressed transcripts belonged to four functional categories: protein
maturation and metabolism (31 ESTs), signalling (22 ESTs), the cell wall (21 ESTs)
and photosynthesis (19 ESTs). 4.4 % (41) of the total ESTs were potentially related
to cell wall formation and maturation. The most highly expressed cell wall EST (15
ESTs) corresponded to a β-xylosidase gene - potentially involved in cell wall remodelling
during growth and development. Other cell wall-related ESTs corresponded to cellulose
synthase, xyloglucan endotranglucosylase/hydrolase (XTH), β-galactosidases, and peroxidases.
The expression patterns of different cell wall-related ESTs were determined at different
developmental stages in flax plants grown under different field conditions. The potential
roles of gene products associated with cell wall related ESTs in fibre cell wall development
is discussed.
Key words
Fibres - flax - cell wall - expressed sequence tags (ESTs) - cellulose - hemicelluloses
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S. Hawkins
Laboratoire de Physiologie des Parois Végétales UPRES EA 3568 USC-INRA
Université des Sciences et Technologies de Lille
59655 Villeneuve d'Ascq
France
Email: simon.hawkins@univ-lille1.fr
Editor: M. Hawkesford