Identification of a t(3;4)(p1.3;q1.5) translocation breakpoint in pigs using somatic cell hybrid mapping and high-resolution mate-pair sequencing.

TitleIdentification of a t(3;4)(p1.3;q1.5) translocation breakpoint in pigs using somatic cell hybrid mapping and high-resolution mate-pair sequencing.
Publication TypeJournal Article
Year of Publication2017
AuthorsFeve, K, Foissac, S, Pinton, A, Mompart, F, Esquerré, D, Faraut, T, Yerle, M, Riquet, J
JournalPLoS One
Volume12
Issue11
Paginatione0187617
Date Published2017
ISSN1932-6203
KeywordsADAMTS Proteins, Animals, Chromosome Mapping, Chromosomes, Mammalian, High-Throughput Nucleotide Sequencing, Models, Genetic, Swine, Translocation, Genetic
Abstract

Reciprocal translocations are the most frequently occurring constitutional structural rearrangements in mammalian genomes. In phenotypically normal pigs, an incidence of 1/200 is estimated for such rearrangements. Even if constitutional translocations do not necessarily induce defects and diseases, they are responsible for significant economic losses in domestic animals due to reproduction failures. Over the last 30 years, advances in molecular and cytogenetic technologies have led to major improvements in the resolution of the characterization of translocation events. Characterization of translocation breakpoints helps to decipher the mechanisms that lead to such rearrangements and the functions of the genes that are involved in the translocation. Here, we describe the fine characterization of a reciprocal translocation t(3;4) (p1.3;q1.5) detected in a pig line. The breakpoint was identified at the base-pair level using a positional cloning and chromosome walking strategy in somatic cell hybrids that were generated from an animal that carries this translocation. We show that this translocation occurs within the ADAMTSL4 gene and results in a loss of expression in homozygous carriers. In addition, by taking this translocation as a model, we used a whole-genome next-generation mate-pair sequencing approach on pooled individuals to evaluate this strategy for high-throughput screening of structural rearrangements.

DOI10.1371/journal.pone.0187617
Alternate JournalPLoS ONE
PubMed ID29121641
PubMed Central IDPMC5679599