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Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors

The first characterised FUSE Binding Protein family member, FUBP1, binds single-stranded DNA to activate MYC transcription. Psi, the sole FUBP protein in Drosophila, binds RNA to regulate P-element and mRNA splicing. Our previous work revealed pro-growth functions for Psi, which depend, in part, on...

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Autores principales: Zaytseva, Olga, Mitchell, Naomi C., Muckle, Damien, Delandre, Caroline, Nie, Zuqin, Werner, Janis K., Lis, John T., Eyras, Eduardo, Hannan, Ross D., Levens, David L., Marshall, Owen J., Quinn, Leonie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110491/
https://www.ncbi.nlm.nih.gov/pubmed/36692218
http://dx.doi.org/10.1242/dev.201563
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author Zaytseva, Olga
Mitchell, Naomi C.
Muckle, Damien
Delandre, Caroline
Nie, Zuqin
Werner, Janis K.
Lis, John T.
Eyras, Eduardo
Hannan, Ross D.
Levens, David L.
Marshall, Owen J.
Quinn, Leonie M.
author_facet Zaytseva, Olga
Mitchell, Naomi C.
Muckle, Damien
Delandre, Caroline
Nie, Zuqin
Werner, Janis K.
Lis, John T.
Eyras, Eduardo
Hannan, Ross D.
Levens, David L.
Marshall, Owen J.
Quinn, Leonie M.
author_sort Zaytseva, Olga
collection PubMed
description The first characterised FUSE Binding Protein family member, FUBP1, binds single-stranded DNA to activate MYC transcription. Psi, the sole FUBP protein in Drosophila, binds RNA to regulate P-element and mRNA splicing. Our previous work revealed pro-growth functions for Psi, which depend, in part, on transcriptional activation of Myc. Genome-wide functions for FUBP family proteins in transcriptional control remain obscure. Here, through the first genome-wide binding and expression profiles obtained for a FUBP family protein, we demonstrate that, in addition to being required to activate Myc to promote cell growth, Psi also directly binds and activates stg to couple growth and cell division. Thus, Psi knockdown results in reduced cell division in the wing imaginal disc. In addition to activating these pro-proliferative targets, Psi directly represses transcription of the growth inhibitor tolkin (tok, a metallopeptidase implicated in TGFβ signalling). We further demonstrate tok overexpression inhibits proliferation, while tok loss of function increases mitosis alone and suppresses impaired cell division caused by Psi knockdown. Thus, Psi orchestrates growth through concurrent transcriptional activation of the pro-proliferative genes Myc and stg, in combination with repression of the growth inhibitor tok.
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spelling pubmed-101104912023-04-19 Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors Zaytseva, Olga Mitchell, Naomi C. Muckle, Damien Delandre, Caroline Nie, Zuqin Werner, Janis K. Lis, John T. Eyras, Eduardo Hannan, Ross D. Levens, David L. Marshall, Owen J. Quinn, Leonie M. Development Research Article The first characterised FUSE Binding Protein family member, FUBP1, binds single-stranded DNA to activate MYC transcription. Psi, the sole FUBP protein in Drosophila, binds RNA to regulate P-element and mRNA splicing. Our previous work revealed pro-growth functions for Psi, which depend, in part, on transcriptional activation of Myc. Genome-wide functions for FUBP family proteins in transcriptional control remain obscure. Here, through the first genome-wide binding and expression profiles obtained for a FUBP family protein, we demonstrate that, in addition to being required to activate Myc to promote cell growth, Psi also directly binds and activates stg to couple growth and cell division. Thus, Psi knockdown results in reduced cell division in the wing imaginal disc. In addition to activating these pro-proliferative targets, Psi directly represses transcription of the growth inhibitor tolkin (tok, a metallopeptidase implicated in TGFβ signalling). We further demonstrate tok overexpression inhibits proliferation, while tok loss of function increases mitosis alone and suppresses impaired cell division caused by Psi knockdown. Thus, Psi orchestrates growth through concurrent transcriptional activation of the pro-proliferative genes Myc and stg, in combination with repression of the growth inhibitor tok. The Company of Biologists Ltd 2023-01-24 /pmc/articles/PMC10110491/ /pubmed/36692218 http://dx.doi.org/10.1242/dev.201563 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Zaytseva, Olga
Mitchell, Naomi C.
Muckle, Damien
Delandre, Caroline
Nie, Zuqin
Werner, Janis K.
Lis, John T.
Eyras, Eduardo
Hannan, Ross D.
Levens, David L.
Marshall, Owen J.
Quinn, Leonie M.
Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
title Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
title_full Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
title_fullStr Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
title_full_unstemmed Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
title_short Psi promotes Drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
title_sort psi promotes drosophila wing growth via direct transcriptional activation of cell cycle targets and repression of growth inhibitors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110491/
https://www.ncbi.nlm.nih.gov/pubmed/36692218
http://dx.doi.org/10.1242/dev.201563
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