Proceedings of
the XLV Italian Society of Agricultural Genetics - SIGA Annual Congress
Salsomaggiore Terme, Italy - 26/29 September, 2001
ISBN 88-900622-1-5
Poster Abstract
THE PGIP GENE
FAMILY SPANS A 50 KB REGION IN THE BEAN GENOME
D’OVIDIO R.*, O’SULLIVAN D.***, ROBERTI
S.*, CAPODICASA C.**, RAIOLA A.**, MELARAGNI M.*, BRANCHER D.*,
DE LORENZO G.**, CERVONE F.**
* Dip. Agrobiologia e Agrochimica,
Università degli Studi della Tuscia, V. S. Camillo De Lellis snc, 01100
Viterbo
dovidio@unitus.it
** Dip. Biologia vegetale ,Università degli
Studi ‘La Sapienza’ di Roma ,P.le Aldo Moro 5, 00185 Roma
*** IARC-Long Ashton Research Station, Bristol, United Kingdom
Polygalacturonase-inhibiting protein, PGIP,
Leucine-rich repeat proteins, defence gene, gene family
Polygalacturonase-inhibiting
protein (PGIP) is a plant cell wall protein that regulates the action of fungal
endopolygalacturonases (PG) favouring the formation of oligogalacturonides
active as elicitors of plant defense responses. On the bases of these
properties, it has been proposed that the PGIP is involved in plant defence
mechanisms.
Genomic analysis
showed that genes encoding PGIPs are organized in gene families and functional
analysis of their encoded products demonstrated that they can have different
recognition capabilities against fungal PG. In bean such specificity can be
controlled by a single amino acid substitution within the predicted b-sheet/b-turn
structure.
In the attempt to
understand better the role of PGIP in plant defence and to identify possible
genetic features of the pgip locus, we have characterized the bean pgip gene
family by isolating and shot-gun sequencing two overlapping BAC clones covering
about 150 Kbp. Sequence analysis of this region revealed that the pgip gene
family is composed by four different members spanning a 50 Kbp region.
Nucleotide sequence comparison of coding regions show a good level of
polymorphism between members of a gene family and a limited variability between
corresponding members of gene family from different bean cultivars. In this
latter case non synonymous substitutions or small deletions are responsible for
sequence variability, and in most case they reside within the predicted
b-sheet/b-turn structure, in position potentially involved in PG recognition.
The genetic
features of the pgip bean locus include the presence of additional ORFs, a
novel 796 bp Mu-like element, a member of a novel family of Ty1-copia
retroelement, Simple Sequence Repeat (SSR) motifs and Tandem Repeats. On a
total of 50 Kbp, about 47 % is annotated and 53 % has to be investigated. The
non-annotated DNA is very rich in AT sequences.
To determine the
extent of recognition specificities contained in a single bean genotype, the
four bean pgip genes are being expressed in PVX to be tested against fungal
Pgs.