A comprehensive study of mammalian SNAG transcription family members
Transcriptional regulation by the family of SNAG (Snail/Gfi-1) zinc fingers has been shown to play a role in various developmental states and diseases. These transcriptional repressors have function in both DNA- and protein-binding, allowing for multiple interactions by a single family member. This...
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ndltd-fau.edu-oai-fau.digital.flvc.org-fau_38452019-07-04T03:51:00Z A comprehensive study of mammalian SNAG transcription family members Chiang, Cindy Chung-Yue. Text Electronic Thesis or Dissertation Florida Atlantic University English xiv, 183 p. : ill. (some col.) electronic Transcriptional regulation by the family of SNAG (Snail/Gfi-1) zinc fingers has been shown to play a role in various developmental states and diseases. These transcriptional repressors have function in both DNA- and protein-binding, allowing for multiple interactions by a single family member. This work aims to characterize the SNAG members Slug, Smuc, Snail, Scratch, Gfi-1, Gfi-1B, and IA-1 in terms of both DNA-protein and protein-protein interactions. The specific DNA sequences to which the zinc finger regions bind were determined for each member, and a general consensus of TGCACCTGTCCGA, was developed for four of the members. Via these studies, we also reveal thebinding affinities of E-box (CANNTG) sequences to the members, since this core is found for multiple members' binding sites. Additionally, protein-protein interactions of SNAG members to other biological molecules were investigated. The Slug domain and Scratch domain have unknown function, yet through yeast two-hybrid screening, we were able to determine protein interaction partners for them as well as for other full length SNAG members. These protein-interacting partners have suggested function as corepressors during transcriptional repression. The comprehensive information determined from these studies allow for a better understanding of the functional relationship between SNAG-ZFPs and other genes. The collected data not only creates a new profile for each member investigated, but it also allows for further studies to be initiated from the results. by Cindy Chiang. Thesis (Ph.D.)--Florida Atlantic University, 2012. Includes bibliography. Electronic reproduction. Boca Raton, Fla., 2012. Mode of access: World Wide Web. Cellular signal transduction Zinc-finger proteins--Synthesis Metalloproteins--Synthesis Genetic transcription--Regulation http://purl.flvc.org/fcla/dt/3342041 794107607 3342041 FADT3342041 fau:3845 Charles E. Schmidt College of Science Department of Biological Sciences http://rightsstatements.org/vocab/InC/1.0/ https://fau.digital.flvc.org/islandora/object/fau%3A3845/datastream/TN/view/comprehensive%20study%20of%20mammalian%20SNAG%20transcription%20family%20members.jpg |
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Cellular signal transduction Zinc-finger proteins--Synthesis Metalloproteins--Synthesis Genetic transcription--Regulation |
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Cellular signal transduction Zinc-finger proteins--Synthesis Metalloproteins--Synthesis Genetic transcription--Regulation A comprehensive study of mammalian SNAG transcription family members |
description |
Transcriptional regulation by the family of SNAG (Snail/Gfi-1) zinc fingers has been shown to play a role in various developmental states and diseases. These transcriptional repressors have function in both DNA- and protein-binding, allowing for multiple interactions by a single family member. This work aims to characterize the SNAG members Slug, Smuc, Snail, Scratch, Gfi-1, Gfi-1B, and IA-1 in terms of both DNA-protein and protein-protein interactions. The specific DNA sequences to which the zinc finger regions bind were determined for each member, and a general consensus of TGCACCTGTCCGA, was developed for four of the members. Via these studies, we also reveal thebinding affinities of E-box (CANNTG) sequences to the members, since this core is found for multiple members' binding sites. Additionally, protein-protein interactions of SNAG members to other biological molecules were investigated. The Slug domain and Scratch domain have unknown function, yet through yeast two-hybrid screening, we were able to determine protein interaction partners for them as well as for other full length SNAG members. These protein-interacting partners have suggested function as corepressors during transcriptional repression. The comprehensive information determined from these studies allow for a better understanding of the functional relationship between SNAG-ZFPs and other genes. The collected data not only creates a new profile for each member investigated, but it also allows for further studies to be initiated from the results. === by Cindy Chiang. === Thesis (Ph.D.)--Florida Atlantic University, 2012. === Includes bibliography. === Electronic reproduction. Boca Raton, Fla., 2012. Mode of access: World Wide Web. |
author2 |
Chiang, Cindy Chung-Yue. |
author_facet |
Chiang, Cindy Chung-Yue. |
title |
A comprehensive study of mammalian SNAG transcription family members |
title_short |
A comprehensive study of mammalian SNAG transcription family members |
title_full |
A comprehensive study of mammalian SNAG transcription family members |
title_fullStr |
A comprehensive study of mammalian SNAG transcription family members |
title_full_unstemmed |
A comprehensive study of mammalian SNAG transcription family members |
title_sort |
comprehensive study of mammalian snag transcription family members |
publisher |
Florida Atlantic University |
url |
http://purl.flvc.org/fcla/dt/3342041 |
_version_ |
1719218926219427840 |