{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T09:25:02Z","timestamp":1787045102763,"version":"build-2736575974"},"posted":{"date-parts":[[2026,8,15]]},"group-title":"Molecular Biology","reference-count":81,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2026,8,15]],"date-time":"2026-08-15T00:00:00Z","timestamp":1786752000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"crossref","award":["R03AG064525"],"award-info":[{"award-number":["R03AG064525"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2026,8,14]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                <jats:p>Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by features of accelerated aging, with a life expectancy of less than two decades. HGPS is commonly caused by a point mutation in the LMNA gene which codes for lamin A, a vital component of the nuclear lamina. The HGPS mutation activates a cryptic splice site and leads to production of a truncated, farnesylated form of lamin A referred to as \"progerin.\" Progerin is also produced in small amounts in healthy individuals and has been implicated in normal aging. HGPS is associated with an accumulation of genomic DNA double-strand breaks (DSBs), and alterations in DSB repair. DSB repair in mammalian cells normally occurs by either homologous recombination (HR), an accurate, templated form of repair, or by DNA end-joining (EJ), a non-templated rejoining of DNA ends. EJ is error-prone, although a portion of EJ events occurs precisely with no alteration to joined sequences. Previously, we reported that over-expression of progerin increased EJ relative to HR and decreased the precision of EJ. In our current work, we designed a novel model experimental system using derivatives of thymidine kinase (tk)-deficient mouse fibroblasts and incorporating a loss-of-function assay to further explore progerin\u2019s impact on EJ. We established cell lines containing an integrated copy of a functional herpes tk gene with an embedded recognition site for endonuclease I-SceI. We examined EJ at the nucleotide level following induction of a DSB within the tk gene by expression of I-SceI and subsequent selection for cells that lost tk gene function. Comparison of EJ products recovered from cells expressing progerin versus from cells not expressing progerin revealed that progerin expression provoked larger DNA deletions associated with DSB repair as well as recovery of multiple repair products from individual cells, suggesting progerin impedes re-joining of DNA ends.<\/jats:p>","DOI":"10.64898\/2026.08.13.744695","type":"posted-content","created":{"date-parts":[[2026,8,15]],"date-time":"2026-08-15T10:30:12Z","timestamp":1786789812000},"source":"Crossref","is-referenced-by-count":0,"title":["Healing of chromosomal breaks is impeded in cells expressing progerin"],"prefix":"10.64898","author":[{"given":"Aubrey A.","family":"Bondurant","sequence":"first","affiliation":[{"name":"Arnold School of Public Health, University of South Carolina, Columbia, South Carolina, United States of America"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emma K.","family":"Grove","sequence":"additional","affiliation":[{"name":"Arnold 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