Proceedings
of the XLVII Italian Society of Agricultural Genetics - SIGA Annual Congress
Verona,
Italy - 24/27 September, 2003
ISBN 88-900622-4-X
Oral
Communication Abstract - S4c
PhEXP18, A PETUNIA ALPHA EXPANSIN GENE: SEEKING FOR
THE FUNCTION
S. ZENONI*, L. REALE**, G. B. TORNIELLI*, L.
LANFALONI***, A. PORCEDDU****, A. FERRARINI*, A. ZAMBONI*, C. MORETTI**, F.
FERRANTI**, M. PEZZOTTI*
*) Dipartimento Scientifico e Tecnologico,
Università degli Studi di Verona
**) Dipartimento di Biologia Vegetale e Biotecnologie
Agroambientali, Università degli Studi di Perugia
***) Dipartimento di Biologia Cellulare e Molecolare,
Università degli Studi di Perugia
****) Istituto di Genetica Vegetale- CNR
cell expansion, cellulose, downregulation,
expansin, Petunia hybrida
In plants, organ
shape is determined by organised and regulated control of cell expansion
together with cell division. Emerging data support the view that the direction
and magnitude of the enlargement of the primary cell wall largely determine the
expansion pattern and thereby the final shape and size of the cells.
Cell wall
proteins are believed to play important roles in regulating cell wall
extensibility which is a key parameter determining cell expansion. Among cell
wall proteins studied to date, expansins are unique in the ability to induce
immediate cell wall extension in vitro and cell expansion in vivo. Expansin
genes have been identified in many plant species and make up a large
superfamily that is divided into two major families, alpha- and beta-expansins,
on the basis of the sequence divergence and biochemical activity. During flower
development, floral organs typically assume their final shape after mitotic
activity has basically ceased, indicating that cell expansion plays an important
role in determining organ shape.
To initiate the
investigation on the function of expansins in vivo and during plant
development, we cloned PhEXP18, a Petunia hybrida
alpha-expansin gene, determined its pattern of spatial and temporal expression
in plant and flower organs and generated transgenic Petunia lines that express
the cDNA encoding PhEXP18 in the antisense orientation under
control of the strong and constitutively expressed cauliflower mosaic virus
(CaMV) 35S promoter. PhEXP18 was expressed mainly in petals,
ovaries and stems. (In petals the expression was higher in the distal portion
(limb) in comparison to the basal portion (tube). Transgenic plants with
reduced PhEXP18 expression levels showed a strong reduction of petal
limb size compared to wild-type. Microscopic observations revealed that
antisense line petal limb epidermal cells were smaller and showed a reduction
in cell wall thickness when compared to wild-type cells. Further analysis
revealed that the reduction in thickness of the antisense line cell walls might
be attributed to a deficiency in crystalline cellulose.