Investigating the Role of FoxO1 in Regulating Protein Synthesis

Bibliographic Details
Main Author: Makey, Nicole Lynne
Language:English
Published: University of Toledo / OhioLINK 2019
Subjects:
Online Access:http://rave.ohiolink.edu/etdc/view?acc_num=toledo156475521794138
id ndltd-OhioLink-oai-etd.ohiolink.edu-toledo156475521794138
record_format oai_dc
spelling ndltd-OhioLink-oai-etd.ohiolink.edu-toledo1564755217941382021-08-03T07:12:14Z Investigating the Role of FoxO1 in Regulating Protein Synthesis Makey, Nicole Lynne Biology Kinesiology Physiology FoxO1 protein synthesis skeletal muscle atrophy muscle physiology Skeletal muscle tissue is a very dynamic and adaptable organ within the human body and is regulated through a balance between protein anabolism and catabolism.It has been well established within the literature that one transcription factor, in particular, FoxO1, plays a role in the regulation of protein degradation. Conversely, there has been some evidence to suggest that FoxO1 might also play a role in the regulation of protein synthesis. Thus, our hypothesis is that the overexpression of FoxO1 influences protein synthesis through both translation efficiency (mTOR signaling), and translation capacity (ribosomal content). To determine the role that FoxO1 has on protein synthesis the gastrocnemius of transgenic mice overexpressing FoxO1 (FoxO1TG) and wild type mice were collected at 24-weeks. To determine rates of protein synthesis, mice were injected with puromycin 30 minutes prior to muscle collection. Furthermore, expression of p70sk6, a key molecule within the mTOR signaling pathway were measured via western blot. Lastly, ribosomal content was assayed by processing tissue with TRIzol and measuring total RNA on a micro-volume plate. Our findings show that FoxO1TG mice did not impact protein synthesis, ii) FoxO1TG mice did, however, cause a significant decrease in total p70s6k, iii) FoxO1TG mice also caused a significant decrease in total RNA content, iv) despite a decrease in total RNA, FoxO1TG did not impact ribosomal rRNA subunits 28S and 18S. The major finding of this study was that the overexpression of FoxO1 does not impact protein synthesis in unchallenged, resting skeletal muscle. 2019-09-05 English text University of Toledo / OhioLINK http://rave.ohiolink.edu/etdc/view?acc_num=toledo156475521794138 http://rave.ohiolink.edu/etdc/view?acc_num=toledo156475521794138 unrestricted This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
collection NDLTD
language English
sources NDLTD
topic Biology
Kinesiology
Physiology
FoxO1
protein synthesis
skeletal muscle atrophy
muscle physiology
spellingShingle Biology
Kinesiology
Physiology
FoxO1
protein synthesis
skeletal muscle atrophy
muscle physiology
Makey, Nicole Lynne
Investigating the Role of FoxO1 in Regulating Protein Synthesis
author Makey, Nicole Lynne
author_facet Makey, Nicole Lynne
author_sort Makey, Nicole Lynne
title Investigating the Role of FoxO1 in Regulating Protein Synthesis
title_short Investigating the Role of FoxO1 in Regulating Protein Synthesis
title_full Investigating the Role of FoxO1 in Regulating Protein Synthesis
title_fullStr Investigating the Role of FoxO1 in Regulating Protein Synthesis
title_full_unstemmed Investigating the Role of FoxO1 in Regulating Protein Synthesis
title_sort investigating the role of foxo1 in regulating protein synthesis
publisher University of Toledo / OhioLINK
publishDate 2019
url http://rave.ohiolink.edu/etdc/view?acc_num=toledo156475521794138
work_keys_str_mv AT makeynicolelynne investigatingtheroleoffoxo1inregulatingproteinsynthesis
_version_ 1719456382817665024