Drosophila HP1 and Insulator Partner Protein 1 (HIPP1) is the homologue of the human co-repressor Chromodomain Y family of proteins that repress neuronal gene expression in mammals. HIPP1 was identified by its extensive co-localization with Heterochromatin Protein 1a (HP1a) in heterochromatic regions of the genome and insulator binding proteins in euchromatic regions. The majority of HIPP1 binding to euchromatin is at binding sites for Drosophila Suppressor of Hairy-wing [Su(Hw)]. Su(Hw) is a zinc finger DNA binding protein that functions as an insulator, activator, and repressor. Transcriptional regulation by Su(Hw) is essential in the ovary and testis, where Su(Hw) functions primarily as a repressor of neuronal genes. However, the mechanism of Su(Hw) dependent repression is not clear. The focus of my thesis work has been defining the role of HIPP1 in development and its contribution to Su(Hw) function and heterochromatin formation. As part of this work, CRISPR was used to generate multiple Hipp1 null alleles and a tagged derivative of the endogenous gene (Hipp1GFP). Hipp1 null flies were found to be viable. Study of HIPP1 expression revealed it is present in most tissues and restricted to the nucleus. HIPP1 showed limited colocalization with HP1a, and tests of repression of transgenes in heterochromatin suggested that HIPP1 is not required for heterochromatin formation. Investigations of HIPP1 binding revealed that Su(Hw) is responsible for the majority of HIPP1 recruitment to euchromatin. Despite this, HIPP1 was found to be dispensable for the transcriptional and insulator functions of Su(Hw) as well as for female and male fertility. These data indicate that HIPP1 is not a critical Su(Hw) cofactor. Further studies are needed to clarify the role of HIPP1 in Drosophila development.
Investigations of HP1 and insulator partner protein 1 (HIPP1)
Abstract
Details
- Title: Subtitle
- Investigations of HP1 and insulator partner protein 1 (HIPP1)
- Creators
- Steve Ehren Glenn - University of Iowa
- Contributors
- Pamela K. Geyer (Advisor)Aloysius J. Klingelhutz (Committee Member)Miles A. Pufall (Committee Member)John R. Manak (Committee Member)Robert A. Cornell (Committee Member)
- Resource Type
- Dissertation
- Degree Awarded
- Doctor of Philosophy (PhD), University of Iowa
- Degree in
- Molecular and Cellular Biology
- Date degree season
- Autumn 2018
- DOI
- 10.17077/etd.wwur-gtke
- Publisher
- University of Iowa
- Number of pages
- vii, 121 pages
- Copyright
- Copyright © 2018 Steve Ehren Glenn
- Language
- English
- Description illustrations
- color illustrations
- Description bibliographic
- Includes bibliographical references (pages 113-121).
- Public Abstract (ETD)
Most cells in the human body have the same genes. The diversity of cell types and tissues arises from controlling the level of expression of genes in different cells. This control is achieved in part through proteins called transcription factors that bind DNA within the genome and either increase or decrease the expression of nearby genes. Many transcription factors have gene specific effects, increasing expression of some genes and decreasing expression of others. The goal of this thesis work is to better understand the underlying principles that determine how transcription factors function to regulate the expression of genes. To accomplish this goal, I studied the fruit fly protein Suppressor of Hairy-wing [Su(Hw)] as a model transcription factor. The primary function of Su(Hw) is to prevent genes that are normally expressed in the brain from being expressed in other tissues. Su(Hw) was shown to interact with an uncharacterized protein, HP1 and Insulator Partner Protein 1 (HIPP1). HIPP1 is the fly version of a human protein, CDYL, that also regulates the expression of neuronal genes. The conservation of HIPP1 from humans to flies suggests that HIPP1 has an important function. This thesis work tested the requirement of HIPP1 in Su(Hw) function and fruit fly development. These studies revealed that Su(Hw) recruits HIPP1 to DNA and that HIPP1 is not required for any identified functions of Su(Hw) or fly survival. By ruling out many predicted functions of HIPP1, these studies may direct future investigations of HIPP1 and transcription factor function.
- Academic Unit
- Craniofacial Anomalies Research Center; Interdisciplinary Graduate Program in Molecular Medicine
- Record Identifier
- 9983776795602771