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Molecular techniques that recover unknown sequences next to a known sequence region have been widely applied in various molecular studies, such as chromosome walking, identification of the insertion site of transposon mutagenesis, fusion gene partner, and chromosomal breakpoints, as well as targeted sequencing library preparation. Although various techniques have been introduced for efficiency enhancement, searching for relevant single molecular event present in a large-sized genome remains challenging. Here, the optimized ligation-mediated polymerase chain reaction (PCR) method was developed and successfully identified chromosomal breakpoints far away from the exon of the new exon junction without the need for nested PCR. In addition to recovering unknown sequences next to a known sequence region, the high efficiency of the method could also improve the performance of targeted next-generation sequencing (NGS).
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http://dx.doi.org/10.1093/biomethods/bpae037 | DOI Listing |
bioRxiv
August 2025
Department of Biology, McMaster University, Hamilton, ON L8S 4K1, Canada.
is a human fungal pathogen capable of both -α and α-α mating and sexual reproduction in laboratory settings. However, the extent of -α and α-α sexual reproductions in natural populations remain unexplored. Here we analyzed the whole-genome sequences of 24 environmental strains of from western Saudi Arabia, including one and 23 α isolates, with 15 α isolates belonging to multi-locus sequence type ST160 as defined by their combined DNA sequences at seven loci.
View Article and Find Full Text PDFGenes Chromosomes Cancer
July 2025
Molecular Biology Laboratory, Instituto Valenciano de Oncología, Valencia, Spain.
We report a uterine myxoid mesenchymal tumor with a novel SS18::VEZF1 gene fusion. The current lesion was identified in a 53-year-old woman who presented with symptomatic "fibroids" showing accelerated growth and heterogeneous morphology on radiologic assessment. Microscopic examination revealed a well-demarcated neoplasm, and the tumor exhibited alternating hypocellular/hyalinized and hypercellular areas, composed of a monomorphic proliferation of spindle, ovoid, and epithelioid cells arranged in sheets.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Emeritus, Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Many genomics specialists recognize that the massive genome rearrangements grouped under the term "chromoanagenesis" are a path to rapid evolutionary change by restructuring chromosomes, creating chimeric sequence combinations, and altering regulatory interactions leading to novel phenotypes. Less attention has been paid to the role of ubiquitous eukaryotic double-strand DNA break repair functions known as "alternative end-joining" (AltEJ) in generating additional DNA sequence innovation. A close look at some examples of chromoanagenesis rearrangements in the human germline and tumor cells illustrates how diverse these novel sequences can be.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Laboratoire de Diagnostic Génétique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Chromoanagenesis correspond to cataclysmic complex chromosomal rearrangements. They are separated into three categories-chromothripsis, chromoanasynthesis, and chromoplexy-based, among others, on the number of breakpoints, the copy number state, and the molecular signature at junctions. However, criteria may be overlapping or may be difficult to evaluate, leading to blurred border between the three types of chromoanagenesis and even other complex chromosomal rearrangements.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Complex chromosomal rearrangements (CCRs), defined as structural variants involving more than two chromosomes or multiple breakpoint junctions, are challenging to resolve, and causal mutations often go unnoticed in genome studies. Short-read whole-genome sequencing enables the characterization of rearrangement junctions in unique sequences. However, issues persist within repetitive regions of the genome, which are prone to rearrangements.
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