BEGIN:VCALENDAR VERSION:2.0 PRODID:-//Biological Sciences - ECPv6.15.18//NONSGML v1.0//EN CALSCALE:GREGORIAN METHOD:PUBLISH X-ORIGINAL-URL:/biology X-WR-CALDESC:Events for Biological Sciences REFRESH-INTERVAL;VALUE=DURATION:PT1H X-Robots-Tag:noindex X-PUBLISHED-TTL:PT1H BEGIN:VTIMEZONE TZID:America/Chicago BEGIN:DAYLIGHT TZOFFSETFROM:-0600 TZOFFSETTO:-0500 TZNAME:CDT DTSTART:20230312T080000 END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0500 TZOFFSETTO:-0600 TZNAME:CST DTSTART:20231105T070000 END:STANDARD BEGIN:DAYLIGHT TZOFFSETFROM:-0600 TZOFFSETTO:-0500 TZNAME:CDT DTSTART:20240310T080000 END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0500 TZOFFSETTO:-0600 TZNAME:CST DTSTART:20241103T070000 END:STANDARD BEGIN:DAYLIGHT TZOFFSETFROM:-0600 TZOFFSETTO:-0500 TZNAME:CDT DTSTART:20250309T080000 END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0500 TZOFFSETTO:-0600 TZNAME:CST DTSTART:20251102T070000 END:STANDARD END:VTIMEZONE BEGIN:VEVENT DTSTART;TZID=America/Chicago:20241115T160000 DTEND;TZID=America/Chicago:20241115T170000 DTSTAMP:20260420T002153 CREATED:20241112T210203Z LAST-MODIFIED:20241112T210203Z UID:10001361-1731686400-1731690000@uwm.edu SUMMARY:Biological Sciences Colloquium: Dr. Chris Quinn DESCRIPTION:Dr. Chris Quinn of UW-Milwaukee will present a talk about his work entitled\, “Harnessing human genetics to investigate the development and degeneration of axons in C. elegans.” \nThe abstract is as follows: \n“Genome sequencing studies have generated a list of de novo variants that are associated with neurodevelopmental disorders such as autism and intellectual disability. However\, little is known about how variants in these genes can disrupt neuronal cell biology to cause defects in neurodevelopment. Our laboratory is using these variants to uncover novel mechanisms that regulate neuronal development in C. elegans. In the first part of this talk\, I will focus on our work with the RBM-26(RBM26/27) RNA binding protein. We found that mutations in rbm-26 cause mitochondrial dysfunction\, axon degeneration and axon targeting defects. Mechanistically\, we discovered that RBM-26 negatively regulates the MALS-1 mitoribosomal assembly factor and that this interaction is required to protect against axon degeneration and axon targeting defects. In the second part\, I will talk about the anc-1 ortholog of SYNE1\, which has been associated with autism and bipolar disorder. We have found that mutations in anc-1 disrupt the polarization of axon growth by disrupting the localization of mitochondria within the neuron. These studies highlight the roles that autism-associated genes can play in promoting mitochondrial function and how disruptions in these processes can lead to the defects in neurodevelopment that underlie autism.” \nThe presentation will begin at 4:00 PM in Lapham Hall N101\, preceded by an informal reception from 3:45 – 4:00 PM. URL:/biology/event/biological-sciences-colloquium-dr-chris-quinn/ LOCATION:Lapham Hall\, N101\, 3209 N Maryland Ave\, Milwaukee\, WI\, 53211\, United States CATEGORIES:Colloquia ATTACH;FMTTYPE=image/jpeg:/biology/wp-content/uploads/sites/21/2024/11/2024-Nov-15-Quinn.jpg X-TRIBE-STATUS: GEO:43.0757204;-87.8840564 X-APPLE-STRUCTURED-LOCATION;VALUE=URI;X-ADDRESS=Lapham Hall N101 3209 N Maryland Ave Milwaukee WI 53211 United States;X-APPLE-RADIUS=500;X-TITLE=3209 N Maryland Ave:geo:-87.8840564,43.0757204 END:VEVENT END:VCALENDAR