{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,24]],"date-time":"2026-08-24T11:23:10Z","timestamp":1787570590909,"version":"build-2736575974"},"reference-count":83,"publisher":"eLife Sciences Publications, Ltd","license":[{"start":{"date-parts":[[2024,1,19]],"date-time":"2024-01-19T00:00:00Z","timestamp":1705622400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2024,1,19]],"date-time":"2024-01-19T00:00:00Z","timestamp":1705622400000},"content-version":"am","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2024,1,19]],"date-time":"2024-01-19T00:00:00Z","timestamp":1705622400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","award":["DK084171"],"award-info":[{"award-number":["DK084171"]}],"id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","award":["DK099134"],"award-info":[{"award-number":["DK099134"]}],"id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000069","name":"National Institute of Arthritis and Musculoskeletal and Skin Diseases","doi-asserted-by":"publisher","award":["AR077533"],"award-info":[{"award-number":["AR077533"]}],"id":[{"id":"10.13039\/100000069","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elifesciences.org"],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>\n                    Genome-wide association studies (GWAS) have identified a large number of candidate genes believed to affect longitudinal bone growth and bone mass. One of these candidate genes,\n                    <jats:italic>TMEM263<\/jats:italic>\n                    , encodes a poorly characterized plasma membrane protein. Single nucleotide polymorphisms in TMEM263 are associated with bone mineral density in humans and mutations are associated with dwarfism in chicken and severe skeletal dysplasia in at least one human fetus. Whether this genotype-phenotype relationship is causal, however, remains unclear. Here, we determine whether and how TMEM263 is required for postnatal growth. Deletion of the\n                    <jats:italic>Tmem263<\/jats:italic>\n                    gene in mice causes severe postnatal growth failure, proportional dwarfism, and impaired skeletal acquisition. Mice lacking Tmem263 show no differences in body weight within the first 2 weeks of postnatal life. However, by P21 there is a dramatic growth deficit due to a disrupted growth hormone (GH)\/insulin-like growth factor 1 (IGF-1) axis, which is critical for longitudinal bone growth.\n                    <jats:italic>Tmem263<\/jats:italic>\n                    -null mice have low circulating IGF-1 levels and pronounced reductions in bone mass and growth plate length. The low serum IGF-1 in\n                    <jats:italic>Tmem263<\/jats:italic>\n                    -null mice is associated with reduced hepatic GH receptor (GHR) expression and GH-induced JAK2\/STAT5 signaling. A deficit in GH signaling dramatically alters GH-regulated genes and feminizes the liver transcriptome of Tmem263-null male mice, with their expression profile resembling wild-type female, hypophysectomized male, and Stat5b-null male mice. Collectively, our data validates the causal role for Tmem263 in regulating postnatal growth and raises the possibility that rare mutations or variants of\n                    <jats:italic>TMEM263<\/jats:italic>\n                    may potentially cause GH insensitivity and impair linear growth.\n                  <\/jats:p>","DOI":"10.7554\/elife.90949","type":"journal-article","created":{"date-parts":[[2023,10,6]],"date-time":"2023-10-06T10:36:29Z","timestamp":1696588589000},"update-policy":"https:\/\/doi.org\/10.7554\/elife.90949","source":"Crossref","is-referenced-by-count":3,"title":["Tmem263 deletion disrupts the GH\/IGF-1 axis and causes dwarfism and impairs skeletal acquisition"],"prefix":"10.7554","volume":"12","author":[{"given":"Dylan C","family":"Sarver","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/00za53h95","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Physiology, Johns Hopkins University School of Medicine","place":["Baltimore, 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