{"id":1934,"date":"2006-06-23T00:00:00","date_gmt":"2006-06-23T07:00:00","guid":{"rendered":"https:\/\/vermont.salk.edu\/news-release\/chewing-up-a-key-regulator-of-fat-synthesis-keeps-mice-lean-despite-a-high-fat-diet\/"},"modified":"2015-12-03T18:08:19","modified_gmt":"2015-12-04T02:08:19","slug":"chewing-up-a-key-regulator-of-fat-synthesis-keeps-mice-lean-despite-a-high-fat-diet","status":"publish","type":"disclosure","link":"https:\/\/www.salk.edu\/es\/news-release\/chewing-up-a-key-regulator-of-fat-synthesis-keeps-mice-lean-despite-a-high-fat-diet\/","title":{"rendered":"Chewing up a key regulator of fat synthesis keeps mice lean despite a high-fat diet"},"content":{"rendered":"<p>La Jolla, CA \u2013 Scientists at the Salk Institute for Biological Studies have  identified a novel pathway that regulates the body&#8217;s ability to store or burn  fat, a discovery that suggests new ways to reduce obesity, diabetes and other  fat-related human diseases. <\/p>\n<p>Genetically engineered mice, in which the pathway was  constantly revved up, were protected from the ravages of a high-fat diet, the  Salk team led by <a href=\"\/es\/faculty\/montminy\/\">Marc Montminy, Ph.D.<\/a>, a professor in  the Clayton Foundation Laboratories for Peptide Biology reports in this week&#8217;s  issue of <em>Ciencia.<\/em><\/p>\n<p>&#8220;These mice were able to deal with a high-fat diet much  better than their normal counterparts,&#8221; Montminy says. &#8220;They  stayed lean and were much more sensitive to insulin, although they ate more,&#8221;  he adds. <\/p>\n<p>In humans, a high-fat diet \u2013 one heavy on red and processed  meats like hot dogs and sausages, refined grains, fried foods and sweets \u2013  increases the risk of fatty liver disease, which may eventually lead to type 2  diabetes, especially in people who are overweight and out of shape. <\/p>\n<p>The engineered mice consumed an equally high-fat diet but  did not gain weight, indicating that fat storage pathways can be tweaked.  &#8220;Maybe the most amazing finding is that these mice are protected from fatty  liver disease, a serious problem in obese individuals with insulin resistance,&#8221;  says Montminy.<\/p>\n<div class=\"imageCaption\"><img decoding=\"async\" src=\"https:\/\/www.salk.eduhttps:\/\/www.salk.edu\/wp-content\/uploads\/2015\/03\/montminy_200606.jpg\" alt=\"Montminy Mice\" \n\n<p>Mice genetically engineered to express permanently elevated levels of TRB3 protein in fat tissue stay lean despite a high-fat diet that puts un-engineered mice on the brink of morbid obesity.<\/p>\n<\/div>\n<p>Our body&#8217;s ability to store fat requires the activity of the  enzyme acetyl-coenzyme A carboxylase, or ACC. When we fast, the body starts to  burn fat while simultaneously shutting down ACC through a chemical modification  called phosphorylation.<\/p>\n<p>The Salk researchers found that a critical protein called  TRB3 orchestrates a second chemical modification of ACC, known as  ubiquitination, which gets rid of the enzyme altogether. &#8220;In this parallel  pathway, TRB3 serves as a go-between for an enzyme that marks ACC for  degradation,&#8221; says Jose Heredia, a graduate student in Montminy&#8217;s lab. <\/p>\n<p>TRB3 levels in adipose tissue usually rise only during  fasting, when ACC should be turned off. Heredia and co-first author Ling Qi,  Ph.D., reasoned that keeping the TRB3 pathway artificially &#8220;on&#8221; during both  fasting and feeding might melt away fat depots.<\/p>\n<p>And that&#8217;s exactly what happened. Mice genetically  engineered to express permanently elevated levels of TRB3 protein in fat tissue  were 10-20 percent skinnier than normal mice. &#8220;Even when we put them on a  high-fat diet, these mice just didn&#8217;t gain any weight,&#8221; says Qi. &#8220;Their  physical activity was the same, but they were constantly burning fat.&#8221;<\/p>\n<p>All this is good news for the fight against obesity and the  disorders characterized by insulin-resistance known as &#8220;metabolic syndrome.&#8221;  Most people with insulin resistance will develop type 2 diabetes within 10  years, unless they lose 5 to 7 percent of their body weight \u2013 about 10 to 15  pounds for someone weighing 200 pounds. Defining how molecules regulating fat  storage interact could lead to novel measures to curb obesity.<\/p>\n<p>Further evidence linking TRB3 to disease comes from recent  findings from a team of Italian scientists who report that mutations in the  human TRB3 gene are associated with several insulin resistance-related health  problems, such as high insulin levels, high cholesterol, and cardiovascular  disease.<\/p>\n<p>Achieving a desired physiological outcome by manipulating  basic biochemistry was clearly satisfying for Montminy. &#8220;What really made this  an interesting story is that the molecular mechanism and the biology  intersected since we were able to explain how TRB3 made the mice lean,&#8221; he  reflects. &#8220;That doesn&#8217;t happen very often.&#8221; <\/p>\n<p>Additional contributors to this study included assistant  professor Robert Screaton, Ph.D., formerly at the Salk, now at Children&#8217;s  Hospital of Eastern Ontario; Judith Y. Altarejos, Ph.D., Naomi Goebel, Michael  Nelson, Ph.D., professor Ronald M. Evans, Ph.D., all at the Salk Institute;  Sherry Niessen, Ian X. MacLeod, and Professor John Yates, Ph. D., from the  Scripps Research Institute in La Jolla, California; Chong Wee Liew, Ph.D., and  assistant professor Rohit Kulkarni, Ph.D., both at the Joslin Diabetes Center  in Boston, Massachusetts; and James Bain, Ph.D., and professor Christopher  Newgard, Ph.D., both at the Sarah W. Stedman Nutrition and Metabolism Center in  Durham, North Carolina.<\/p>\n<p>The Salk Institute for Biological  Studies in La Jolla, California, is an independent nonprofit organization  dedicated to fundamental discoveries in the life sciences, the improvement of  human health and the training of future generations of researchers. Jonas Salk,  M.D., whose polio vaccine all but eradicated the crippling disease  poliomyelitis in 1955, opened the Institute in 1965 with a gift of land from  the City of San Diego  and the financial support of the March of Dimes.<\/p>","protected":false},"featured_media":0,"template":"","faculty":[100],"disease-research":[],"class_list":["post-1934","disclosure","type-disclosure","status-publish","hentry","faculty-marc-montminy"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Chewing up a key regulator of fat synthesis keeps mice lean despite a high-fat diet - Salk Institute for Biological Studies<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.salk.edu\/es\/news-release\/chewing-up-a-key-regulator-of-fat-synthesis-keeps-mice-lean-despite-a-high-fat-diet\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Chewing up a key regulator of fat synthesis keeps mice lean despite a high-fat diet - 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