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Drosophila Uri, a PP1α binding protein, is essential for viability, maintenance of DNA integrity and normal transcriptional activity

Background Protein phosphatase 1 (PP1) is involved in diverse cellular processes, and is targeted to substrates via interaction with many different protein binding partners. PP1 catalytic subunits (PP1c) fall into PP1 alpha and PP1 beta subfamilies based on sequence analysis, however very few PP1c b...

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Published in:BMC molecular biology 2008-04, Vol.9 (1), p.36-36, Article 36
Main Authors: Kirchner, Jasmin, Vissi, Emese, Gross, Sascha, Szoor, Balazs, Rudenko, Andrey, Alphey, Luke, White-Cooper, Helen
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cited_by cdi_FETCH-LOGICAL-b524t-a8f8de0fc307d8ee43f4ea16c503dc84554add892145a2d5ba6ee5e178e7594f3
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container_end_page 36
container_issue 1
container_start_page 36
container_title BMC molecular biology
container_volume 9
creator Kirchner, Jasmin
Vissi, Emese
Gross, Sascha
Szoor, Balazs
Rudenko, Andrey
Alphey, Luke
White-Cooper, Helen
description Background Protein phosphatase 1 (PP1) is involved in diverse cellular processes, and is targeted to substrates via interaction with many different protein binding partners. PP1 catalytic subunits (PP1c) fall into PP1 alpha and PP1 beta subfamilies based on sequence analysis, however very few PP1c binding proteins have been demonstrated to discriminate between PP1 alpha and PP1 beta . Results URI (unconventional prefoldin RPB5 interactor) is a conserved molecular chaperone implicated in a variety of cellular processes, including the transcriptional response to nutrient signalling and maintenance of DNA integrity. We show that Drosophila Uri binds PP1 alpha with much higher affinity than PP1 beta , and that this ability to discriminate between PP1c forms is conserved to humans. Most Uri is cytoplasmic, however we found some protein associated with active RNAPII on chromatin. We generated a uri loss of function allele, and show that uri is essential for viability in Drosophila. uri mutants have transcriptional defects, reduced cell viability and differentiation in the germline, and accumulate DNA damage in their nuclei. Conclusion Uri is the first PP1 alpha specific binding protein to be described in Drosophila. Uri protein plays a role in transcriptional regulation. Activity of uri is required to maintain DNA integrity and cell survival in normal development.
doi_str_mv 10.1186/1471-2199-9-36
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PP1 catalytic subunits (PP1c) fall into PP1 alpha and PP1 beta subfamilies based on sequence analysis, however very few PP1c binding proteins have been demonstrated to discriminate between PP1 alpha and PP1 beta . Results URI (unconventional prefoldin RPB5 interactor) is a conserved molecular chaperone implicated in a variety of cellular processes, including the transcriptional response to nutrient signalling and maintenance of DNA integrity. We show that Drosophila Uri binds PP1 alpha with much higher affinity than PP1 beta , and that this ability to discriminate between PP1c forms is conserved to humans. Most Uri is cytoplasmic, however we found some protein associated with active RNAPII on chromatin. We generated a uri loss of function allele, and show that uri is essential for viability in Drosophila. uri mutants have transcriptional defects, reduced cell viability and differentiation in the germline, and accumulate DNA damage in their nuclei. 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PP1 catalytic subunits (PP1c) fall into PP1 alpha and PP1 beta subfamilies based on sequence analysis, however very few PP1c binding proteins have been demonstrated to discriminate between PP1 alpha and PP1 beta . Results URI (unconventional prefoldin RPB5 interactor) is a conserved molecular chaperone implicated in a variety of cellular processes, including the transcriptional response to nutrient signalling and maintenance of DNA integrity. We show that Drosophila Uri binds PP1 alpha with much higher affinity than PP1 beta , and that this ability to discriminate between PP1c forms is conserved to humans. Most Uri is cytoplasmic, however we found some protein associated with active RNAPII on chromatin. We generated a uri loss of function allele, and show that uri is essential for viability in Drosophila. uri mutants have transcriptional defects, reduced cell viability and differentiation in the germline, and accumulate DNA damage in their nuclei. 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PP1 catalytic subunits (PP1c) fall into PP1 alpha and PP1 beta subfamilies based on sequence analysis, however very few PP1c binding proteins have been demonstrated to discriminate between PP1 alpha and PP1 beta . Results URI (unconventional prefoldin RPB5 interactor) is a conserved molecular chaperone implicated in a variety of cellular processes, including the transcriptional response to nutrient signalling and maintenance of DNA integrity. We show that Drosophila Uri binds PP1 alpha with much higher affinity than PP1 beta , and that this ability to discriminate between PP1c forms is conserved to humans. Most Uri is cytoplasmic, however we found some protein associated with active RNAPII on chromatin. We generated a uri loss of function allele, and show that uri is essential for viability in Drosophila. uri mutants have transcriptional defects, reduced cell viability and differentiation in the germline, and accumulate DNA damage in their nuclei. 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subjects Drosophila
Gene expression
Genetic aspects
Phosphatases
Physiological aspects
title Drosophila Uri, a PP1α binding protein, is essential for viability, maintenance of DNA integrity and normal transcriptional activity
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