Data di Pubblicazione:
2013
Abstract:
Molecular defects occurring in the endothelin receptor type-
B (EDNRB) gene are known to be associated with pigmentary
anomalies and intestinal aganglionosis in humans, rodents
and horses. We carried out a cytogenetic investigation in 2
ewes heterozygous for the deletion of the EDNRB gene and
in 2 more females as control. The RBA-banding showed that
all 4 ewes were karyologically normal. EDNRB gene-specific
probes were produced by PCR and cloning. The application
of the R-banding and propidium iodide-staining fluorescent
in situ hybridization allowed mapping the gene to OAR
10q22 and confirmed the heterozygous status of the ewes
investigated for the EDNRB gene deletion. For the fine estimation
of the gene length in sheep and for the correct sizing
of the chromosomal gap, a dual-color FISH was applied to
high-resolution DNA fibers in combination with digital imaging
microscopy. The comparison of the DNA fiber barcodes
indicated a chromosomal deletion larger than the
EDNRB gene itself. The length of the gene, not known for
sheep until now, was estimated to be ~ 21 kb, whereas the
microchromosomal deletion was ~ 100 kb. EDNRB is located
in a chromosomal region previously shown to be a fragile
site. The applied method allowed locating the potential
breakpoints, thus permitting further interesting prospective
investigations also in the field of the fragile sites in sheep.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Breakpoints; Chromatin fibers; EDNRB; Fluorescence in situ hybridization; Sheep Lethal white syndrome
Elenco autori:
Pauciullo, Alfredo
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