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Cancer genomes are characterized by the accumulation of small-scale somatic mutations as well as large-scale chromosomal deletions, amplifications, and complex structural rearrangements. This characteristic is at least partially dependent on the ability of cancer cells to undergo recurrent chromosome breakage. In order to address the extent to which chromosomal structural rearrangement breakpoints correlate with recurrent DNA double-strand breaks (DSBs), we simultaneously mapped chromosome structural variation breakpoints (using whole-genome DNA-seq) and spontaneous DSB formation (using Break-seq) in the estrogen receptor (ER)-positive breast cancer cell line MCF-7 and a non-cancer control breast epithelium cell line MCF-10A. We identified concurrent DSBs and structural variation breakpoints almost exclusively in the pericentromeric region of chromosome 16q in MCF-7 cells. We fine-tuned the identification of copy number variation breakpoints on 16q. In addition, we detected recurrent DSBs that occurred in both MCF-7 and MCF-10A. We propose a model for DSB-driven chromosome rearrangements that lead to the translocation of 16q, likely with 10q, and the eventual 16q loss that does not involve the pericentromere of 16q. We present evidence from RNA-seq data that select genes, including SHCBP1, ORC6, and MYLK3, which are immediately downstream from the 16q pericentromere, show heightened expression in MCF-7 cell line compared to the control. Data published by The Cancer Genome Atlas show that all three genes have increased expression in breast tumor samples. We found that SHCBP1 and ORC6 are both strong poor prognosis and treatment outcome markers in the ER-positive breast cancer cohort. We suggest that these genes are potential oncogenes for breast cancer progression. The search for tumor suppressor loss that accompanies the 16q loss ought to be augmented by the identification of potential oncogenes that gained expression during chromosomal rearrangements.
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http://dx.doi.org/10.3390/genes13071228 | DOI Listing |
Front Genet
August 2025
Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Background And Objective: Parental chromosomal structural variations (SVs) represent a primary genetic factor contributing to recurrent spontaneous abortion (RSA). Individuals carrying SVs with complex chromosomal rearrangements (CCRs) typically exhibit a normal phenotype but are at an increased risk of miscarriage. Current standard clinical detection methods are insufficient for the identification and interpretation of all SV types, particularly complex and occult SVs, thereby presenting a significant challenge for clinical genetic counseling.
View Article and Find Full Text PDFYing Yong Sheng Tai Xue Bao
July 2025
Ecological Restoration and Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610213, China.
Urban forest parks play a pivotal role in maintaining urban ecological security. The dynamics in fractional vegetation coverage (FVC) are key indicators for evaluating their ecological restoration effectiveness and sustainable management. Based on normalized difference vegetation index data of Chengdu Longquan Mountain Urban Forest Park from Landsat satellites spanning from 1993 to 2023, we used a comprehensive suite of analytical methods including Theil-Sen median slope estimation, Median-Kendall trend tests, additive seasonal and trend breakpoint detection, and the optimal partial geo-detector model (OPGD) to analyze both linear and nonlinear spatiotemporal variations of FVC within the park as well as driving factors.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Division of Molecular Genetics, Center for Medical Science, Fujita Health University, Aichi, Japan.
Long-read sequencers are known for their effectiveness in detecting genomic structural variations (SV) and are becoming a standard approach for comprehensive genetic analysis. In preimplantation genetic testing (PGT) for SV carriers, information on breakpoint junctions is required to determine the carrier status in embryo selection. Long-read sequencers are employed for SV cases that are difficult to analyze with conventional cytogenetical methods and the detailed SV junction information they provide yields valuable insights.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Departments of Biochemistry, Molecular Biology and Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Clinical diagnostic workflows have been focused on exome sequencing and the detection of small protein-coding variants (single-nucleotides, short insertions, and deletions) often overlooking complex genomic rearrangements (CGR). Indeed, detection of CGRs required genome rather than exome sequencing and development of advanced analytical tools. Among the available technologies for genome sequencing, short-read whole genome sequencing (srWGS) is currently the most cost-efficient technology for detecting variants as it covers most of the genome and theoretically allows the detection of the whole spectrum of genomic variations.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Chromoanagenesis encompasses catastrophic genomic rearrangements, with chromoanasynthesis referring to unbalanced germline events involving one or multiple chromosomes, distinct from the mostly balanced rearrangements seen in cancer-associated chromothripsis and chromoplexy. Initially identified via chromosomal microarray analysis (CMA) and custom high-density arrays, chromoanasynthesis detection and delineation was improved by next-generation sequencing (NGS). However, the short read-lengths and read-depth variations of NGS limit its fine-mapping capabilities.
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