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DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm

Development of the Drosophila visceral muscle depends on Anaplastic Lymphoma Kinase (Alk) receptor tyrosine kinase (RTK) signaling, which specifies founder cells (FCs) in the circular visceral mesoderm (VM). Although Alk activation by its ligand Jelly Belly (Jeb) is well characterized, few target mo...

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Autores principales: Mendoza-Garcia, Patricia, Basu, Swaraj, Sukumar, Sanjay Kumar, Arefin, Badrul, Wolfstetter, Georg, Anthonydhason, Vimala, Molander, Linnea, Uçkun, Ezgi, Lindehell, Henrik, Lebrero-Fernandez, Cristina, Larsson, Jan, Larsson, Erik, Bemark, Mats, Palmer, Ruth H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722224/
https://www.ncbi.nlm.nih.gov/pubmed/34905617
http://dx.doi.org/10.1242/dev.199465
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author Mendoza-Garcia, Patricia
Basu, Swaraj
Sukumar, Sanjay Kumar
Arefin, Badrul
Wolfstetter, Georg
Anthonydhason, Vimala
Molander, Linnea
Uçkun, Ezgi
Lindehell, Henrik
Lebrero-Fernandez, Cristina
Larsson, Jan
Larsson, Erik
Bemark, Mats
Palmer, Ruth H.
author_facet Mendoza-Garcia, Patricia
Basu, Swaraj
Sukumar, Sanjay Kumar
Arefin, Badrul
Wolfstetter, Georg
Anthonydhason, Vimala
Molander, Linnea
Uçkun, Ezgi
Lindehell, Henrik
Lebrero-Fernandez, Cristina
Larsson, Jan
Larsson, Erik
Bemark, Mats
Palmer, Ruth H.
author_sort Mendoza-Garcia, Patricia
collection PubMed
description Development of the Drosophila visceral muscle depends on Anaplastic Lymphoma Kinase (Alk) receptor tyrosine kinase (RTK) signaling, which specifies founder cells (FCs) in the circular visceral mesoderm (VM). Although Alk activation by its ligand Jelly Belly (Jeb) is well characterized, few target molecules have been identified. Here, we used targeted DamID (TaDa) to identify Alk targets in embryos overexpressing Jeb versus embryos with abrogated Alk activity, revealing differentially expressed genes, including the Snail/Scratch family transcription factor Kahuli (Kah). We confirmed Kah mRNA and protein expression in the VM, and identified midgut constriction defects in Kah mutants similar to those of pointed (pnt). ChIP and RNA-Seq data analysis defined a Kah target-binding site similar to that of Snail, and identified a set of common target genes putatively regulated by Kah and Pnt during midgut constriction. Taken together, we report a rich dataset of Alk-responsive loci in the embryonic VM and functionally characterize the role of Kah in the regulation of embryonic midgut morphogenesis.
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spelling pubmed-87222242022-01-26 DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm Mendoza-Garcia, Patricia Basu, Swaraj Sukumar, Sanjay Kumar Arefin, Badrul Wolfstetter, Georg Anthonydhason, Vimala Molander, Linnea Uçkun, Ezgi Lindehell, Henrik Lebrero-Fernandez, Cristina Larsson, Jan Larsson, Erik Bemark, Mats Palmer, Ruth H. Development Research Article Development of the Drosophila visceral muscle depends on Anaplastic Lymphoma Kinase (Alk) receptor tyrosine kinase (RTK) signaling, which specifies founder cells (FCs) in the circular visceral mesoderm (VM). Although Alk activation by its ligand Jelly Belly (Jeb) is well characterized, few target molecules have been identified. Here, we used targeted DamID (TaDa) to identify Alk targets in embryos overexpressing Jeb versus embryos with abrogated Alk activity, revealing differentially expressed genes, including the Snail/Scratch family transcription factor Kahuli (Kah). We confirmed Kah mRNA and protein expression in the VM, and identified midgut constriction defects in Kah mutants similar to those of pointed (pnt). ChIP and RNA-Seq data analysis defined a Kah target-binding site similar to that of Snail, and identified a set of common target genes putatively regulated by Kah and Pnt during midgut constriction. Taken together, we report a rich dataset of Alk-responsive loci in the embryonic VM and functionally characterize the role of Kah in the regulation of embryonic midgut morphogenesis. The Company of Biologists Ltd 2021-12-14 /pmc/articles/PMC8722224/ /pubmed/34905617 http://dx.doi.org/10.1242/dev.199465 Text en © 2021. 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
Mendoza-Garcia, Patricia
Basu, Swaraj
Sukumar, Sanjay Kumar
Arefin, Badrul
Wolfstetter, Georg
Anthonydhason, Vimala
Molander, Linnea
Uçkun, Ezgi
Lindehell, Henrik
Lebrero-Fernandez, Cristina
Larsson, Jan
Larsson, Erik
Bemark, Mats
Palmer, Ruth H.
DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm
title DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm
title_full DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm
title_fullStr DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm
title_full_unstemmed DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm
title_short DamID transcriptional profiling identifies the Snail/Scratch transcription factor Kahuli as an Alk target in the Drosophila visceral mesoderm
title_sort damid transcriptional profiling identifies the snail/scratch transcription factor kahuli as an alk target in the drosophila visceral mesoderm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722224/
https://www.ncbi.nlm.nih.gov/pubmed/34905617
http://dx.doi.org/10.1242/dev.199465
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