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In this paper, we developed a highly sensitive approach to detect interchromosomal rearrangements in cattle by searching for abnormal linkage disequilibrium patterns between markers located on different chromosomes in large paternal half-sib families genotyped as part of routine genomic evaluations. We screened 5571 families of artificial insemination sires from 15 breeds and revealed 13 putative interchromosomal rearrangements, 12 of which were validated by cytogenetic analysis and long-read sequencing. These consisted of one Robertsonian fusion, 10 reciprocal translocations, and the first case of insertional translocation reported in cattle. Taking advantage of the wealth of data available in cattle, we performed a series of complementary analyses to define the exact nature of these rearrangements, investigate their origins, and search for factors that may have favored their occurrence. We also evaluated the risks to the livestock industry and showed significant negative effects on several traits in the sires and in their balanced or aneuploid progeny compared with wild-type controls. Thus, we present the most comprehensive and thorough screen for interchromosomal rearrangements compatible with normal spermatogenesis in livestock species. This approach is readily applicable to any population that benefits from large genotype data sets, and will have direct applications in animal breeding. Finally, it also offers interesting prospects for basic research by allowing the detection of smaller and rarer types of chromosomal rearrangements than GTG banding, which are interesting models for studying gene regulation and the organization of genome structure.
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http://dx.doi.org/10.1101/gr.277787.123 | DOI Listing |
Genome structural variants (SVs) comprise a sizable portion of functionally important genetic variation in all organisms; yet, many SVs evade discovery using short reads. While long-read sequencing can find the hidden SVs, the role of SVs in variation in organismal traits remains largely unclear. To address this gap, we investigate the molecular basis of 50 classical phenotypes in 11 strains using highly contiguous genome assemblies generated with Oxford Nanopore long reads.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain.
Chromoanagenesis events have been identified in chronic lymphocytic leukemia (CLL), the most common leukemia in Western countries. Among the three events included within this term, chromothripsis is the most frequently reported. Its prevalence in CLL is low, ranging from 1 to 3% of patients in unselected cohorts, and it has been associated with poor prognostic factors, such as abnormal TP53 and genomic complexity, and dismal outcome.
View Article and Find Full Text PDFNew Phytol
October 2025
National Engineering Research Center of JUNCAO Technology, College of Juncao Science and Ecology, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Many pathogenic fungi display 'two-speed genome', with the fast-evolving genomic compartments enriched with repetitive sequences, particularly the transposons, which have been shown to drive the variation of pathogenicity-associated genes. Supernumerary chromosomes (SCs) are known to facilitate genomic variation in fungal pathogens, but their specific role in such processes remains understudied. In this study, we assessed the transferability of SCs between asexual Magnaporthe oryzae strains during co-culture and co-infection, and investigated their role in genome reconstruction through experimental evolution assays.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, USA.
The fungal genus includes several life-threatening human pathogens as well as diverse saprobic species whose genome architecture, ecology, and evolutionary history remain less well characterized. Understanding how some lineages evolved into major pathogens remains a central challenge and may be advanced by comparisons with their nonpathogenic counterparts. Integrative approaches have become essential for delimiting species and reconstructing evolutionary relationships, particularly in lineages with cryptic diversity or extensive chromosomal rearrangements.
View Article and Find Full Text PDFFront Plant Sci
June 2025
School of Life Sciences, Jiangsu Normal University, Xuzhou, Jiangsu, China.
Introduction: Previous phylogenetic studies of Ipomoeeae species have shown inconsistent results, and latest molecular analyses have classified this tribe into two major clades (Argyreiinae and Astripomoeinae) comprising seven smaller clades. The cross-species chromosome painting (CCP) analysis can offer valuable insights into the phylogenetic relationships among species.
Methods: Here, we analyzed representative species from each small clade using CCP with oligonucleotide (oligo) probes derived from chromosomes 7 (7-1/7-2) and 15 (15-1/15-2) of to further elucidate their phylogenetic relationships.