{"id":2,"date":"2023-08-14T22:19:30","date_gmt":"2023-08-15T05:19:30","guid":{"rendered":"http:\/\/labs.wsu.edu\/jiyue-zhu\/?page_id=2"},"modified":"2025-04-30T12:21:03","modified_gmt":"2025-04-30T19:21:03","slug":"sample-page","status":"publish","type":"page","link":"https:\/\/labs.wsu.edu\/jiyue-zhu\/","title":{"rendered":""},"content":{"rendered":"<div class=\"wsu-hero wsu-width--full wsu-pattern--wsu-light-radial-left wsu-hero--size-small wsu-zindex--level-0 wsu-hide--tablet-medium \">\n\t\n\t<div class=\"wsu-image-frame wsu-image-frame--fill\">\n\t<img decoding=\"async\" src=\"https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg\"\n\t\tsrcset=\"https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg 1892w, https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg 396w, https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg 792w, https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg 198w, https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg 768w, https:\/\/wpcdn.web.wsu.edu\/wp-labs\/uploads\/sites\/3323\/2023\/11\/mice-ESC-1.jpg 1536w\"\n\t\tsizes=\"(max-width: 1892px) 100vw, 1892px\"\n\t\talt=\"Telomere\"\n\t\tstyle=\"object-position: 79% 67%\"\n\t\t\/>\n<\/div>\n\n\t<div class=\"wsu-overlay wsu-pattern-after wsu-overlay--none wsu-pattern--none\"><\/div>\n\t<div class=\"wsu-hero__content\">\n\t\t<div class=\"wsu-hero__caption\">\n\t\t\t\t\t\t\t\t\t<div id=\"title-id-69d3969e1ed43\" class=\"wsu-title wsu-hero__title\"><span>Our aim<\/span><\/div>\n\t\t\t\t\t\t\t\t\t<div class=\"wsu-caption wsu-hero__copy\">\n\t\t\t\t<strong>Decoding Chromosomal Ends: Evolution and Enhanced Animal Models for Unraveling Human Cancer, Aging, and Age-Related Diseases<\/strong>\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t<\/div>\n<\/div>\n\n\n<h2><b>Research Summary<\/b><\/h2>\n<h3><em>1. Regulation of Telomerase<\/em><\/h3>\n<p>Because most adult human cells lack telomerase activity, as they go through successive cell divisions, their telomeres gradually shorten. Ultimately, this leads to replicative senescence. In contrast to adult human cells, high levels of telomerase activity are prevalent in 90% of cancerous and immortal human cells. For decades, it has been known that the <i>TERT<\/i> gene is subject to stringent repression and human cells rarely evade senescence. The Zhu lab is dedicated to deciphering the mechanisms accountable for establishing and sustaining this repressive state of the <i>TERT<\/i> gene during development, as well as its expression in cancer cells and normal proliferating tissues.<\/p>\n<h3><em>2. Mouse Models of Human Diseases: Bridging Gaps in Physiology<\/em><\/h3>\n<p>Mouse models have proven indispensable in biomedical research, providing invaluable insights into human diseases. However, disparities in human and murine physiology can hinder the translation of discoveries from mouse models into human clinical trials. Telomere biology presents a prime example because of the significant differences in telomere length and telomerase expression between mice and humans. While most human somatic cells lack telomerase expression and have short telomeres (ranging 5-15 kb), adult mouse cells universally express telomerase and possess very long telomeres (\u2265 50 kb). This contrast contributes to the distinct tendency of human and mouse somatic cells to undergo telomere-driven replicative senescence, a phenomenon implicated in impaired tissue regeneration, aging, and age-associated disorders.<\/p>\n<p>In the pursuit of refining mouse models for studying aging and age-related ailments, we have developed a genetically engineered mouse strain called HuT mice, aimed at embodying human-like telomere homeostasis. The concept underlying HuT mice builds upon two decades of comprehensive research into the genetic and epigenetic regulation of the human <i>TERT<\/i> (<i>hTERT<\/i>) gene during cellular differentiation and development. Leveraging these insights, we strategically incorporated human regulatory elements of <i>hTERT<\/i> into the mouse <i>Tert<\/i> locus (<i>mTert<\/i>), resulting in a humanized <i>mTert<\/i> gene: <i>hmTert<\/i>. These genetically engineered HuT mice (<em>Tert<sup>h\/h<\/sup><\/em>) exhibit little telomerase activity in most adult tissues and are born with telomeres measuring less than 10 kb \u2014 faithfully mimicking human telomere homeostasis. This groundbreaking HuT model holds significant implications for studying cancer and other age-related diseases, offering a dependable platform for unraveling the complexities of human physiology in the context of aging.<\/p>\n<section class=\"row single gutter pad-top\">\n<div class=\"column two\">\n<h2>Areas of Current Research Focus in the Laboratory<\/h2>\n<ul>\n<li>Genetic and epigenetic regulation of the human telomerase gene during development and cell differentiation<\/li>\n<li>Development of HuT mice: A mouse strain with humanized telomere homeostasis<\/li>\n<li>Study of cellular senescence in mouse cells with human-like short telomeres<\/li>\n<li>Assessing the influence of humanized telomeres on mouse lifespan and health-span<\/li>\n<li>Exploration of innovative strategies for melanoma prevention and treatment through the utilization of HuT mice<\/li>\n<\/ul>\n<h2><b>Current Research Funding<\/b><\/h2>\n<ul>\n<li><strong>National Institute on Aging, 2022-2027<\/strong><\/li>\n<li><strong>National Institute of General Medical Sciences, 2023-2028<\/strong><\/li>\n<li><strong>Department of Defense (DoD) Congressionally Directed Medical Research Program (CDMRP), 2023-2027<\/strong><\/li>\n<\/ul>\n<\/div>\n<\/section>\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Research Summary 1. Regulation of Telomerase Because most adult human cells lack telomerase activity, as they go through successive cell divisions, their telomeres gradually shorten. Ultimately, this leads to replicative senescence. In contrast to adult human cells, high levels of telomerase activity are prevalent in 90% of cancerous and immortal human cells. For decades, it [&hellip;]<\/p>\n","protected":false},"author":24922,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"categories":[1],"tags":[],"wsuwp_university_location":[],"wsuwp_university_org":[],"_links":{"self":[{"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/pages\/2"}],"collection":[{"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/users\/24922"}],"replies":[{"embeddable":true,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/comments?post=2"}],"version-history":[{"count":19,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/pages\/2\/revisions"}],"predecessor-version":[{"id":164,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/pages\/2\/revisions\/164"}],"wp:attachment":[{"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/media?parent=2"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/categories?post=2"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/tags?post=2"},{"taxonomy":"wsuwp_university_location","embeddable":true,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/wsuwp_university_location?post=2"},{"taxonomy":"wsuwp_university_org","embeddable":true,"href":"https:\/\/labs.wsu.edu\/jiyue-zhu\/wp-json\/wp\/v2\/wsuwp_university_org?post=2"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}