Cargando…

Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization

Cilia have evolved hugely diverse structures and functions to participate in a wide variety of developmental and physiological processes. Ciliary specialization requires differences in gene expression, but few transcription factors are known to regulate this, and their molecular function is unclear....

Descripción completa

Detalles Bibliográficos
Autores principales: Newton, Fay G., zur Lage, Petra I., Karak, Somdatta, Moore, Daniel J., Göpfert, Martin C., Jarman, Andrew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414849/
https://www.ncbi.nlm.nih.gov/pubmed/22698283
http://dx.doi.org/10.1016/j.devcel.2012.05.010
_version_ 1782240270548467712
author Newton, Fay G.
zur Lage, Petra I.
Karak, Somdatta
Moore, Daniel J.
Göpfert, Martin C.
Jarman, Andrew P.
author_facet Newton, Fay G.
zur Lage, Petra I.
Karak, Somdatta
Moore, Daniel J.
Göpfert, Martin C.
Jarman, Andrew P.
author_sort Newton, Fay G.
collection PubMed
description Cilia have evolved hugely diverse structures and functions to participate in a wide variety of developmental and physiological processes. Ciliary specialization requires differences in gene expression, but few transcription factors are known to regulate this, and their molecular function is unclear. Here, we show that the Drosophila Forkhead box (Fox) gene, fd3F, is required for specialization of the mechanosensory cilium of chordotonal (Ch) neurons. fd3F regulates genes for Ch-specific axonemal dyneins and TRPV ion channels, which are required for sensory transduction, and retrograde transport genes, which are required to differentiate their distinct motile and sensory ciliary zones. fd3F is reminiscent of vertebrate Foxj1, a motile cilia regulator, but fd3F regulates motility genes as part of a broader sensory regulation program. Fd3F cooperates with the pan-ciliary transcription factor, Rfx, to regulate its targets directly. This illuminates pathways involved in ciliary specialization and the molecular mechanism of transcription factors that regulate them.
format Online
Article
Text
id pubmed-3414849
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-34148492012-08-20 Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization Newton, Fay G. zur Lage, Petra I. Karak, Somdatta Moore, Daniel J. Göpfert, Martin C. Jarman, Andrew P. Dev Cell Article Cilia have evolved hugely diverse structures and functions to participate in a wide variety of developmental and physiological processes. Ciliary specialization requires differences in gene expression, but few transcription factors are known to regulate this, and their molecular function is unclear. Here, we show that the Drosophila Forkhead box (Fox) gene, fd3F, is required for specialization of the mechanosensory cilium of chordotonal (Ch) neurons. fd3F regulates genes for Ch-specific axonemal dyneins and TRPV ion channels, which are required for sensory transduction, and retrograde transport genes, which are required to differentiate their distinct motile and sensory ciliary zones. fd3F is reminiscent of vertebrate Foxj1, a motile cilia regulator, but fd3F regulates motility genes as part of a broader sensory regulation program. Fd3F cooperates with the pan-ciliary transcription factor, Rfx, to regulate its targets directly. This illuminates pathways involved in ciliary specialization and the molecular mechanism of transcription factors that regulate them. Cell Press 2012-06-12 /pmc/articles/PMC3414849/ /pubmed/22698283 http://dx.doi.org/10.1016/j.devcel.2012.05.010 Text en © 2012 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Newton, Fay G.
zur Lage, Petra I.
Karak, Somdatta
Moore, Daniel J.
Göpfert, Martin C.
Jarman, Andrew P.
Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization
title Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization
title_full Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization
title_fullStr Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization
title_full_unstemmed Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization
title_short Forkhead Transcription Factor Fd3F Cooperates with Rfx to Regulate a Gene Expression Program for Mechanosensory Cilia Specialization
title_sort forkhead transcription factor fd3f cooperates with rfx to regulate a gene expression program for mechanosensory cilia specialization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414849/
https://www.ncbi.nlm.nih.gov/pubmed/22698283
http://dx.doi.org/10.1016/j.devcel.2012.05.010
work_keys_str_mv AT newtonfayg forkheadtranscriptionfactorfd3fcooperateswithrfxtoregulateageneexpressionprogramformechanosensoryciliaspecialization
AT zurlagepetrai forkheadtranscriptionfactorfd3fcooperateswithrfxtoregulateageneexpressionprogramformechanosensoryciliaspecialization
AT karaksomdatta forkheadtranscriptionfactorfd3fcooperateswithrfxtoregulateageneexpressionprogramformechanosensoryciliaspecialization
AT mooredanielj forkheadtranscriptionfactorfd3fcooperateswithrfxtoregulateageneexpressionprogramformechanosensoryciliaspecialization
AT gopfertmartinc forkheadtranscriptionfactorfd3fcooperateswithrfxtoregulateageneexpressionprogramformechanosensoryciliaspecialization
AT jarmanandrewp forkheadtranscriptionfactorfd3fcooperateswithrfxtoregulateageneexpressionprogramformechanosensoryciliaspecialization