Proceedings
of the XLVI Italian Society of Agricultural Genetics - SIGA Annual Congress
Giardini
Naxos, Italy - 18/21 September, 2002
ISBN 88-900622-3-1
Poster
Abstract - 1.10
GENETIC DIVERSITY AND
CULTIVAR IDENTIFICATION IN OLIVE BY MICROSATELLITE MARKERS
MONTEMURRO C.*, PASQUALONE A.**, SIMEONE R.*, FERRARA E.***, BLANCO A.*
*) Dipartimento di Biologia e Chimica Agro-forestale ed ambientale (Di.B.C.A.), Università di Bari
**) Dipartimento di Progettazione e Gestione dei Sistemi Agro-zootecnici e forestali (Pro.Ge.S.A.), Università di Bari
***) Dipartimento di Scienze delle Produzioni Vegetali, Università di Bari
Olea europaea L., microsatellite markers,
genetic diversity
Olive (Olea europaea L.) is a cultivated species for the
production of high quality oil for human consumption. The crop, distibuted
throughout the Mediterranean basin, presents a very high number of cultivars
difficult to recognize on the basis of morpho-physiological traits, so that
some cases of homonymy and synonymy still exist. Molecular markers are
independent by environmental conditions and are characterised by higher
polymorphisms than morphological and biochemical markers. Some kinds of
molecular markers, such as RAPDs, AFLPs and ISSRs, have been proposed and used
to achieve a better distinction of cultivars as well as to assess the genetic
variability of wild and cultivated germplasm. Recently microsatellite markers
have been developed in O. europaea . The aim of this research was to use
microsatellite markers to assess the genetic distances within a representative
sample of Mediterranean germplasm as well as to distinguish olive cultivars. A
total of 60 cultivars native of Italy, Spain, France and Greece was analyzed
with sixty eight primers pairs of microsatellite markers; primer sequences were
described by Sefc et al. (2000), Carriero et al.
(2002), Cipriani et al. (2002) and Maggini (personal
communication). A preliminary screening was done on a set of 15 cultivars to
choose the most polymorphic primers, and thus avoiding useless amplifications.
Amplified fragments ranged from 110 to 300 bp and a mean ratio of polymorphic
bands/amplified bands of 0,46 was found. A dendrogram of genetic distances was
elaborated and almost all the cultivars resulted to be distinguishable with a
few cases of probable homonymy. This study enabled the assessment of genetic
relationships and the discrimination of the cultivars. The accurate cultivar
identification is necessary to satisfy the requirements of the Community
Directive (Dir. 92/34, 93/48, 93/64, 93/79 CEE) for the marketing of C.A.C.
(Community Agriculture Conformitas) plant material.
References:
Carriero F.
Fontanazza G. Cellini F. Giorio G.,2002. Identification of simple sequence repeats (SSRs) in olive (Olea europaea L.). Theoretical Applied Genetics 104:
301-307.
Cipriani G.
Marrazzo M.T. Marconi R. Cimato A. Testolin R., 2002. Microsatellite markers isolated in olive (Olea europaea L.) suitable for individual fingerprinting
and reveal polymorphism within ancient cultivars. Theoretical Applied
Genetics 104: 223-228.
Sefc
K.M., Lopes M.S., Mendoca D., Rodrigues Dos Santos M., Laimer Da Camara Machado
M., Da Camara Machado A.., 2000. Identification of microsatellite loci in olive
(Olea europaea L.) and their characterization
in Italian and Iberian olive trees. Molecular
Ecology 9 (8): 1171-1173