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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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. |
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en en_US |
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Others
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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 |
_version_ |
1716574936679579648 |