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 - 1.33
GENETIC
ANALYSIS OF NEW VIVIPAROUS MUTANTS OF MAIZE
A.
GIULINI*, G. CONSONNI*, F. DALLA VECCHIA**, N. RASCIO**, N. LA ROCCA**, R.
PILU*, S. STEFANELLI***, R. TUBEROSA***, G. GAVAZZI*
*)
Department of Crop Production, Via Celoria 2, 20133 Milano, Italy
**)
Department of Biology, Via Colombo 3, 35121 Padova, Italy
***)
Department of Agroenvironmental Sciences and Technology, Via Farin 44, 40127
Bologna, Italy
abscisic acid,
maize, viviparous mutants
Abscissic
acid (ABA) regulates many agronomically important aspects of plant development,
including synthesis of seed storage proteins and lipids, promotion of seed
desiccation tolerance and dormancy. In addition, ABA mediates some
physiological responses to environmental stresses such as stomatal closure, or
induction of tolerance to water. Mutants, altered in ABA metabolism, provide a
good opportunity to identify which functions at the molecular, biochemical,
cellular and/or whole plant level are affected by impaired ABA biosynthesis or
sensitivity.
We
selected out of a large sample of vp mutants,
originated in our lab or received from other scientists, four mutants yielding
green seedlings. The majority of the vp mutants in maize
are associated to white or pale yellow endosperm and seedling because they are
due to a mutational event occurring in the first part of the biosynthetic route
that is shared by ABA biosynthesis and carotenogenesis.
The
mutants thus selected and provisionally symbolized vp374*, vp390*, vp105*,
vp D*, affect in downstream steps of the biosynthesis or they
represent regulatory genes involved in the perception and/or transduction of
ABA signal.
They
were intercrossed to establish their allelism relationship and crossed to vp1, a
regulatory gene of the ABA signal and to vp13, a mutant
specific of the ABA biosynthesis.
Double
mutants vp1/vpD* and vp1/vp105* were also
tested. We will present data on their response to exogenous ABA, on their
endogenous ABA content, on their pattern of ABA inducible genes during embryo
maturation.
Their
analysis will be extended to vegetative tissues to establish how the mutation
affects water loss and stomatal aperture with the aim to establish whether the
genes under study are specifically expressed during embryogenesis or if they
are also important during vegetative growth.