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UID:1153@biology.technion.ac.il

DTSTART;TZID=Asia/Jerusalem:20230123T130000

DTEND;TZID=Asia/Jerusalem:20230123T140000

DTSTAMP:20230112T082313Z

URL:https://biology.technion.ac.il/en/seminars/dr-tomer-shpilka-department
 -of-molecular-cell-and-cancer-biology-at-the-university-of-massachusetts-c
 han-medical-school/

SUMMARY:Dr. Tomer Shpilka - Department of Molecular\, Cell and Cancer Biolo
 gy at the University of Massachusetts Chan Medical School [No Categories]
DESCRIPTION:Location: Faculty Of Biology Auditorium  Dr. Tomer Shpilka\n Af
 filiation: \n Host:Prof. Benjamin Podbilewicz  \n The UPRmt coordinates mi
 tochondrial network expansion and peroxisome biogenesis in the model organ
 ism Caenorhabditis elegans\n\nAs organisms develop\, individual cells gene
 rate mitochondria and peroxisomes to fulfill their physiological requireme
 nts. A decline\, or dysfunction in these organelles is associated with age
 ing and a vast array of clinical manifestations including metabolic disord
 ers and neurodegenerative diseases. Despite this\, it is unknown how mitoc
 hondrial network expansion and peroxisome biogenesis is scaled to cell gro
 wth\, and what compensatory pathways cells employ to maintain the organell
 es’ function. The mitochondrial unfolded protein response (UPRmt) is a s
 ignaling pathway mediated by the transcription factor ATFS-1. Using geneti
 c and biochemical approaches in the model organism Caenorhabditis elegans 
 we demonstrate that ATFS-1 mediates an adaptable mitochondrial network exp
 ansion and peroxisome biogenesis program that is active throughout normal 
 development. We characterized the molecular mechanism and signaling events
  that regulate the UPRmt and uncovered a peroxisomal retrograde response t
 hat is required for peroxisome biogenesis. These findings as well as the t
 herapeutic potential and future directions of my studies will be presented
 .\n\n&nbsp\;\n\n&nbsp\; 
LOCATION:Faculty Of Biology Auditorium

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DTSTART:20221030T010000

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