{"id":2167,"date":"2012-03-29T15:20:12","date_gmt":"2012-03-29T19:20:12","guid":{"rendered":"http:\/\/therapytoronto.ca\/news\/?p=2167"},"modified":"2012-03-30T20:24:07","modified_gmt":"2012-03-31T00:24:07","slug":"researchers-look-at-genes-for-learning-remembering-forgetting","status":"publish","type":"post","link":"https:\/\/therapytoronto.ca\/news\/2012\/03\/researchers-look-at-genes-for-learning-remembering-forgetting\/","title":{"rendered":"Researchers look at genes for learning, remembering, forgetting"},"content":{"rendered":"<p>From the University of Utah press release via EurekAlert!:<\/p>\n<blockquote><p><strong><img loading=\"lazy\" class=\"alignright\" title=\"brain\" src=\"http:\/\/therapytoronto.ca\/images\/blogpics\/Brain.jpg\" alt=\"\" width=\"200\" height=\"200\" \/>Certain genes and proteins that promote growth and development of embryos also play a surprising role in sending chemical signals that help adults learn, remember, forget and perhaps become addicted<\/strong>, University of Utah biologists have discovered.<\/p>\n<p>&#8220;We found that these molecules and signaling pathways [named Wnt] do not retire after development of the organism, but have a new and surprising role in the adult. <strong>They are called back to action to change the properties of the nervous system in response to experience<\/strong>,&#8221; says biology Professor Andres Villu Maricq, senior author of the new study in the March 30 issue of the journal <em>Cell<\/em>.<\/p>\n<p>The study was performed in C. elegans \u2013 the millimeter-long roundworm or nematode \u2013 which has a nervous system that serves as a model for those of vertebrate animals, including humans.<\/p>\n<p>Because other Wnt pathways in worms are known to work in humans too, the researchers believe that Wnt genes, the Wnt proteins they produce and so-called &#8220;Wnt signaling&#8221; also are involved in human learning, memory and forgetting.<\/p>\n<p>&#8220;Almost certainly what we have discovered is going on in our brain as well,&#8221; Maricq says. And because a worm nerve-signal &#8220;receptor&#8221; in the study is analogous to a human nicotine receptor involved in addiction, schizophrenia and some other mental disorders, some of the genes identified in the worm study &#8220;represent possible new targets for treatment of schizophrenia and perhaps addiction,&#8221; he adds.<\/p>\n<p>Wnt genes and their proteins already were known to &#8220;pattern the development and distribution of organs in the body&#8221; during embryo development, and to be responsible for various cancers and developmental defects when mutated, he says.<\/p>\n<p>Maricq conducted the study with these Utah biologists: doctoral students Michael Jensen and Dane Maxfield; postdoctoral researchers Michael M. Francis, Frederic Hoerndli and Rui Wang; undergraduate Erica Johnson; Penelope Brockie, a research associate professor; and David M. Madsen, a senior research specialist. The study was funded by the National Institutes of Health and the American Heart Association.<\/p>\n<p><strong>Synapse Plasticity is the Basis of Learning and Memory<\/strong><\/p>\n<p>Synapses are the connections between nerve cells (neurons). Nerve signals are transmitted through synapses. <strong>Learning and memory concern how these connections are made, broken, strengthened or weakened<\/strong>. Proteins known as receptors are delivered to the synapses or removed from them to strengthen or weaken the connection.<\/p>\n<p>In the new study, Maricq and colleagues identified a &#8220;Wnt signaling pathway&#8221; \u2013 a series of genes and the proteins they produce \u2013 that controls the strength of nerve signal transmission from one neuron through a synapse to the next neuron. This allows &#8220;plasticity&#8221; of synapses \u2013 a key factor in learning, retaining memories and forgetting.<\/p>\n<p>&#8220;The adult nervous system is not a stagnant tissue, but rather dynamic and plastic, with the strength of synapses \u2013 specialized neuron-to-neuron connections \u2013 changing with experience, learning and memory,&#8221; Maricq says. &#8220;It&#8217;s not a fixed thing, like when you&#8217;re done making the heart, you&#8217;re done.&#8221;<\/p>\n<p><strong>When synapses and thus incoming nerve signals are strengthened by adding receptors, an organism learns and remembers; when the opposite occurs, the organism forgets<\/strong>, he adds.<\/p>\n<p>How is that connection strengthened or weakened? When one neuron sends a nerve signal to another neuron, the first neuron releases a chemical known as a neurotransmitter, which moves through the synapse connecting the two cells and attaches or binds to receptors on the surface of the second neuron.<\/p>\n<p>&#8220;You can think of the receptors like amplifiers, like hearing aids,&#8221; Maricq says.<\/p>\n<p>The volume of the received nerve signal depends on the number of receptors, which are stored in a supply depot just below the nerve cell&#8217;s surface.<\/p>\n<p>The Wnt signaling identified in the new study &#8220;tells the depot to put more receptors into the synapse \u2013 or not,&#8221; says Maricq.<\/p>\n<p>He emphasizes that the Wnt chemical signal is different than the actual nerve signal carried by a neurotransmitter chemical, which in the new study was acetylcholine. The Wnt signal &#8220;is a secondary signal that controls the volume of the neurotransmitter signal,&#8221; Maricq says.<\/p>\n<p><strong>Worms Reveal Details of Nerve Signal Volume Control<\/strong><\/p>\n<p>By crippling various genes in the worms, the researchers identified the &#8220;signaling pathway&#8221; by which a Wnt protein in one nerve cell sends a chemical signal to another cell telling it to increase the number of receptors on its surface, thus increasing the strength or volume of nerve signals between the cells.<\/p>\n<p>The type of nerve-signal receptor in the study is an acetylcholine receptor named ACR-16. When researchers crippled the gene that makes the ACR-16 receptor protein, there were not enough receptors, so nerve signals were disrupted and the worms &#8220;had uncoordinated movement,&#8221; Maricq says. &#8220;They were semi-paralyzed.&#8221;<\/p>\n<p>The scientists found mutations of other genes that also resulted in inadequate ACR-16 receptors and impaired the worms&#8217; movement. They discovered such genes belong to the &#8220;Wnt signaling pathway&#8221; that puts enough receptors on the cell surface so signals can be received.<\/p>\n<p>Besides ACR-16, genes in that pathway produced proteins named CWN-2 \u2013 which is a Wnt protein \u2013 LIN-17, CAM-1 and DSH-1.<\/p>\n<p>Here is how that pathway controls the volume of incoming nerve signals:<\/p>\n<ol>\n<li>A neuron releases CWN-2, which binds onto a receptor protein on the signal-receiving cell. That protein is a newly discovered combination of the LIN-17 and CAM-1 proteins.<\/li>\n<li>The LIN-17\/CAM-1 protein sends a signal to a protein called disheveled, or DSH-1.<\/li>\n<li>&#8220;DSH-1 somehow sends the volume-control signal&#8221; that dispatches more ACR-16 receptors from depots inside the second neuron to that cell&#8217;s surface, thus boosting the volume of the received nerve signal, Maricq says.<\/li>\n<\/ol>\n<p>The researchers used a green jellyfish protein to mark the ACR-16 receptors so they were visible under a microscope. When any of the genes in the Wnt signaling pathway were mutant, the scientists could see the green-labeled receptors accumulate under the surfaces of nerve cells instead of moving to the surface.<\/p>\n<p>Another experiment recorded electrical currents in worm nerve synapses and found it was smaller when any of the Wnt pathway genes were mutated. The smaller current \u2013 reflecting impaired nerve-signal transmission \u2013 explains why the mutant worms were partially paralyzed.<\/p>\n<p><strong>Human Version of Worm Receptor Tied to Mental Disorders<\/strong><\/p>\n<p>The ACR-16 acetylcholine receptor is the worm version of the alpha-7 nicotinic acetylcholine receptor in humans and other vertebrates. Both are similar in structure and function in animals from worms to fruit flies, mice and people.<\/p>\n<p><strong>The alpha-7 receptor &#8220;is important in schizophrenia and a number of different mental disorders, and may have a role in addiction<\/strong>, but we don&#8217;t understand how it&#8217;s regulated,&#8221; Maricq says.<\/p>\n<p>Many existing psychiatric drugs modify synapse strength. The new study suggests research should be done to show if the same Wnt signaling genes in worms also control alpha-7 receptor levels on human brain cells. If so, new drugs might be developed to target those genes as a way to treat mental disorders, including addiction.<\/p>\n<p>&#8220;Addiction is like learning at a primitive level,&#8221; Maricq says. &#8220;Addiction means that somewhere in your brain, synapses are too strong. So you want more.&#8221;<\/p><\/blockquote>\n<!-- AddThis Advanced Settings generic via filter on the_content --><!-- AddThis Share Buttons generic via filter on the_content -->","protected":false},"excerpt":{"rendered":"<p>From the University of Utah press release via EurekAlert!: Certain genes and proteins that promote growth and development of embryos also play a surprising role in sending chemical signals that&#8230; <a class=\"read-more-link\" href=\"https:\/\/therapytoronto.ca\/news\/2012\/03\/researchers-look-at-genes-for-learning-remembering-forgetting\/\">Read more &raquo;<\/a><!-- AddThis Advanced Settings generic via filter on get_the_excerpt --><!-- AddThis Share Buttons generic via filter on get_the_excerpt --><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[4],"tags":[19,49],"_links":{"self":[{"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/posts\/2167"}],"collection":[{"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/comments?post=2167"}],"version-history":[{"count":1,"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/posts\/2167\/revisions"}],"predecessor-version":[{"id":2168,"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/posts\/2167\/revisions\/2168"}],"wp:attachment":[{"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/media?parent=2167"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/categories?post=2167"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/therapytoronto.ca\/news\/wp-json\/wp\/v2\/tags?post=2167"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}