Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes

Fibroblast growth factor-2 (FGF-2) is a multifunctional factor which is found in 21-25 kDa high molecular weight (HMW), or 16-18 kDa low molecular weight (LMW) forms, resulting from translation initiation from unconventional CUG- or conventional AUG- start sites, respectively. Previous studies have...

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Main Author: Sun, Guangping
Format: Others
Language:en
en_US
Published: 2007
Online Access:http://hdl.handle.net/1993/2388
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-MWU.anitoba.ca-dspace#1993-23882013-01-11T13:30:06ZSun, Guangping2007-06-01T19:23:26Z2007-06-01T19:23:26Z1999-09-01T00:00:00Zhttp://hdl.handle.net/1993/2388Fibroblast growth factor-2 (FGF-2) is a multifunctional factor which is found in 21-25 kDa high molecular weight (HMW), or 16-18 kDa low molecular weight (LMW) forms, resulting from translation initiation from unconventional CUG- or conventional AUG- start sites, respectively. Previous studies have demonstrated that rat HMW- but not LMW-FGF-2, introduced into cardiac myocytes by gene transfer, caused a distinct nuclear phenotype, characterized by condensed chromatin and formation of several DNA 'clumps' inside the nucleus. In the present study we investigated first whether human HMW FGF-2, sharing 82% homology with its rat counterpart at the CUG-initiated extension, was also capable of eliciting the same phenotype as rat HMW FGF-2. Secondly, we investigated whether the mechanism of chromatin condensation and separation caused by HMW FGF-2 engaged an apoptosis-like, mechanism. Finally, we examined whether the HMW FGF-2 induced nuclear phenotype resulted from a mitosis-like mechanism. (Abstract shortened by UMI.)4375344 bytes184 bytesapplication/pdftext/plainenen_USChromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytesHuman Anatomy & Cell ScienceM.Sc.
collection NDLTD
language en
en_US
format Others
sources NDLTD
description Fibroblast growth factor-2 (FGF-2) is a multifunctional factor which is found in 21-25 kDa high molecular weight (HMW), or 16-18 kDa low molecular weight (LMW) forms, resulting from translation initiation from unconventional CUG- or conventional AUG- start sites, respectively. Previous studies have demonstrated that rat HMW- but not LMW-FGF-2, introduced into cardiac myocytes by gene transfer, caused a distinct nuclear phenotype, characterized by condensed chromatin and formation of several DNA 'clumps' inside the nucleus. In the present study we investigated first whether human HMW FGF-2, sharing 82% homology with its rat counterpart at the CUG-initiated extension, was also capable of eliciting the same phenotype as rat HMW FGF-2. Secondly, we investigated whether the mechanism of chromatin condensation and separation caused by HMW FGF-2 engaged an apoptosis-like, mechanism. Finally, we examined whether the HMW FGF-2 induced nuclear phenotype resulted from a mitosis-like mechanism. (Abstract shortened by UMI.)
author Sun, Guangping
spellingShingle Sun, Guangping
Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes
author_facet Sun, Guangping
author_sort Sun, Guangping
title Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes
title_short Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes
title_full Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes
title_fullStr Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes
title_full_unstemmed Chromatin condensation and fragmentation caused by CUG-initiated FGF-2 in cardiomyocytes
title_sort chromatin condensation and fragmentation caused by cug-initiated fgf-2 in cardiomyocytes
publishDate 2007
url http://hdl.handle.net/1993/2388
work_keys_str_mv AT sunguangping chromatincondensationandfragmentationcausedbycuginitiatedfgf2incardiomyocytes
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