Show simple item record

dc.contributor.authorBhattacharya, Asmita
dc.date.accessioned2019-10-15T16:47:13Z
dc.date.available2020-08-29T06:00:39Z
dc.date.issued2019-08-30
dc.identifier.otherBhattacharya_cornellgrad_0058F_11717
dc.identifier.otherhttp://dissertations.umi.com/cornellgrad:11717
dc.identifier.otherbibid: 11050466
dc.identifier.urihttps://hdl.handle.net/1813/67493
dc.description.abstractRecent literature has revolutionized our view on the patho-physiological importance and the underlying molecular mechanism of endoplasmic reticulum (ER)-associated degradation (ERAD) in health and disease. Aside from being a downstream element of ER stress response or the unfolded protein response (UPR), ERAD also plays a direct and vital role in health and disease, in a substrate-specific and largely UPR-independent manner. The Sel1L-Hrd1 complex is the most conserved branch of mammalian endoplasmic reticulum (ER)-associated degradation (ERAD) machinery.  Here, we have focused on the role of ERAD in the liver in the context of energy metabolism, bile homeostasis and cancer pathogenesis. In a recent publication, we reported the discovery of a novel mechanism underlying ERAD-mediated regulation of Fgf21 expression during growth and fasting-feeding.  Mice with liver-specific deletion of Sel1L exhibit growth retardation with markedly elevated circulating Fgf21, leading to massive alterations in growth and systemic metabolic profile.  Mechanistically, we show that the Sel1L-Hrd1 ERAD complex controls Fgf21 transcription by regulating the ubiquitination and turnover (and thus nuclear abundance) of ER-resident transcription factor Crebh.  This study not only establishes the importance of hepatic Sel1L-Hrd1 ERAD in the regulation of systemic energy metabolism, but also reveals a novel hepatic “ERAD-Crebh-Fgf21” axis directly linking ER protein turnover to gene transcription and systemic metabolic regulation.  In another study, our data revealed the importance of ERAD in the regulation of bile metabolism, where a deficiency in hepatic ERAD causes significantly impaired secretion of bile acids, cholesterol and phosphatidylcholine into bile, leading to hypercholanemia and extreme sensitivity to dietary bile acid challenge. This occurs due to defective maturation of exporter proteins associated with bile production, owing to faulty ERAD of these proteins. Finally, in a parallel study, we identify and characterize a novel and significant relationship between hepatic ERAD and liver cancer pathogenesis via the Wnt signalling pathway. Here we demonstrate that Sel1L-Hrd1 ERAD in the liver functions to triage the secreted protein Wnt5A during its maturation in the ER. In the absence of ERAD, Wnt5A aggregates and allows unrestrained proliferation of hepatocytes, thereby markedly increasing the propensity to liver cancer development.  Taken together, we propose the new concept of “constitutive” or “basal” ERAD and its significance in managing cellular and organismal function, and define novel paradigms underlying ERAD function in both quality and quantity control of proteins synthesized in the ER, and nuclear gene transcription.
dc.language.isoen_US
dc.subjectFgf21
dc.subjectprotein folding
dc.subjectWnt pathway
dc.subjectBiochemistry
dc.subjectphysiology
dc.subjectMolecular biology
dc.subjectERAD
dc.subjectcancer
dc.subjectbile
dc.titleENDOPLASMIC RETICULUM ASSOCIATED DEGRADATION (ERAD) IN THE LIVER
dc.typedissertation or thesis
thesis.degree.disciplineGenetics, Genomics and Development
thesis.degree.grantorCornell University
thesis.degree.levelDoctor of Philosophy
thesis.degree.namePh.D., Genetics, Genomics and Development
dc.contributor.chairWeiss, Robert S.
dc.contributor.committeeMemberQi, Ling
dc.contributor.committeeMemberSimpson, Kenneth William
dc.contributor.committeeMemberKurpios, Natasza
dcterms.licensehttps://hdl.handle.net/1813/59810
dc.identifier.doihttps://doi.org/10.7298/k4gs-zj35


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Statistics