{"id":583,"date":"2018-06-12T16:27:16","date_gmt":"2018-06-12T16:27:16","guid":{"rendered":"https:\/\/psblab.org\/?p=583"},"modified":"2018-06-12T16:27:16","modified_gmt":"2018-06-12T16:27:16","slug":"atf5-mitoupr-pre-print","status":"publish","type":"post","link":"https:\/\/psblab.org\/?p=583","title":{"rendered":"ATF5 mitoUPR pre-print"},"content":{"rendered":"<p>Our paper on the role of ATF5 in the mammalian mitochondrial unfolded protein response (UPRmt) is now on BioRxiv as a <a href=\"https:\/\/www.biorxiv.org\/content\/early\/2018\/06\/12\/344606\">pre-print<\/a>. It&#8217;s also been submitted to a regular journal, so hopefully will be in press some time this millenium.<\/p>\n<p>For the uninitiated, UPRmt is a mitochondrion specific unfolded protein response, much of which was figured out in worms (<em>C. elegans<\/em>). The key mediator is the transcription factor<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC2846537\/\"> ATFS1<\/a>, which has both mito&#8217; and nuclear targeting domains. It is normally made and imported into mito&#8217;s and destroyed by proteases. When mito&#8217; proteostasis is upset (e.g., a mis-match in stoichiometry between the mtDNA and nuclear DNA encoded subunits of the electron transport chain, which causes the leftover bits to mis-fold or aggregate), the import is blocked and ATFS1 goes to the nucleus. There, it upregulates a bunch of things to restore mito&#8217; homestasis including chaperones, antioxidants, and glycolysis to take care of energy needs while the mito&#8217;s are undergoing repair.<\/p>\n<p>All those things (chaperones, antioxidants, glycolysis) sound like they might be useful to have around in a situation such as cardiac ischemia (i.e., <a href=\"https:\/\/psblab.org\/?page_id=10\">what we study<\/a>), so we reasoned that activating mito-UPR might be cardioprotective. To induce it in mice, we used oligomycin (yes, that ATP synthase inhibitor) or doxycycline (a tetracycline antibiotic that <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/26475870\">disrupts<\/a> mito&#8217; ribosomes &#8211; which is a good reason not to use it in experiments). Sure enough, after 6 hours (as expected for a gene program) the hearts were protected against ischemia-reperfusion injury.<\/p>\n<p>Within the mito&#8217; UPR field there&#8217;s a debate about what the mammalian ortholog of the worm ATFS1 protein is. Some folks have said the mito UPR is perhaps just a branch of the integrated stress response, mediated mainly by <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/28566324\">ATF4<\/a>. This has been accompanied by a general perception in the field that maybe mito UPR is<em> just a worm thing<\/em> and might not really exist in mammals at all?\u00a0 That changed a couple of years ago when our collaborator Cole Haynes <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/27426517\">showed<\/a> that the mammalian trasncription factor ATF5 can rescue the ATFS1 knockout worm.<\/p>\n<p>So, we tested the UPRmt inducers for cardioprotection in an <em>Atf5<\/em>-\/- mouse, and the protection was lost. To the best of our knowledge, this is the first in-vivo demonstration that ATF5 is a component of the mito&#8217; UPR in mammals (previously it had been shown in cell culture).\u00a0 We also did some RNA-Seq, trying to find out the pathways induced, and while we did see the classical UPRmt target genes such as <em>hsp60<\/em> were up by qPCR, there wasn&#8217;t really much going on in the seq&#8217; data &#8211; certainly no gene signatures or big pathways. In some ways this is a good thing &#8211; it would be kinda boring if we just saw an ISR or Nrf2\/Keap or NFKB or any of those other &#8220;classical&#8221; stress signatures. Instead, it&#8217;s likely we&#8217;ll have to drill down at the individual target level to really identify the downstream molecular mechanism by which ATF5 is inducing protection.<\/p>\n<p>The other interesting aside to this paper, is there&#8217;s quite a sizeable <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=doxycycline+AND+ischemia+AND+(heart+OR+cardiac)\">literature<\/a> on the use of tetracycline antibiotics for cardioprotection, including some human <a href=\"https:\/\/clinicaltrials.gov\/ct2\/show\/NCT00469261\">clinical trials<\/a>. To date, the party line has been that doxycycline confers protection by <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/21689755\">inhibiting matrix metalloproteases<\/a> (they&#8217;re induced during and after heart attack). But, our data showing a requirement of ATF5 for dox-induced protection suggests an alternative mechanism.<\/p>\n<p>Finally, a note on the practicalities of this operation.\u00a0 The paper&#8217;s lead author, Yves Wang, undertook a Herculean effort just to get the study done, because the <em>Atf5<\/em>-\/- mice are a total nightmare to deal with!\u00a0 Due to an olfactory neural defect, the homozygotes exhibit ~80% neonatal mortality &#8211; the pups can&#8217;t find the teat and so can&#8217;t get milk. As such, the vivarium bill for maintaining the <em>Atf5<\/em>-\/- colony is currently running about $2500 a month, even with our exceptionally low <a href=\"https:\/\/www.urmc.rochester.edu\/animal-resource\/charges.aspx\">per-diem rates<\/a>. Hopefully once this is published we can down-size a bit!<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Our paper on the role of ATF5 in the mammalian mitochondrial unfolded protein response (UPRmt) is now on BioRxiv as a pre-print. It&#8217;s also been submitted to a regular journal, so hopefully will be in press some time this millenium. &hellip; <a href=\"https:\/\/psblab.org\/?p=583\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-583","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/psblab.org\/index.php?rest_route=\/wp\/v2\/posts\/583","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/psblab.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/psblab.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/psblab.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/psblab.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=583"}],"version-history":[{"count":1,"href":"https:\/\/psblab.org\/index.php?rest_route=\/wp\/v2\/posts\/583\/revisions"}],"predecessor-version":[{"id":584,"href":"https:\/\/psblab.org\/index.php?rest_route=\/wp\/v2\/posts\/583\/revisions\/584"}],"wp:attachment":[{"href":"https:\/\/psblab.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=583"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/psblab.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=583"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/psblab.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=583"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}