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Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation
The MCM2-7 complex is a highly conserved hetero-hexameric protein complex, critical for DNA unwinding at the replicative fork during DNA replication. Overexpression or mutation in MCM2-7 genes is linked to and may drive several cancer types in humans. In mice, mutations in MCM2-7 genes result in gro...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258838/ https://www.ncbi.nlm.nih.gov/pubmed/35737938 http://dx.doi.org/10.1371/journal.pgen.1010255 |
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author | Rubio-Ferrera, Irene Baladrón-de-Juan, Pablo Clarembaux-Badell, Luis Truchado-Garcia, Marta Jordán-Álvarez, Sheila Thor, Stefan Benito-Sipos, Jonathan Monedero Cobeta, Ignacio |
author_facet | Rubio-Ferrera, Irene Baladrón-de-Juan, Pablo Clarembaux-Badell, Luis Truchado-Garcia, Marta Jordán-Álvarez, Sheila Thor, Stefan Benito-Sipos, Jonathan Monedero Cobeta, Ignacio |
author_sort | Rubio-Ferrera, Irene |
collection | PubMed |
description | The MCM2-7 complex is a highly conserved hetero-hexameric protein complex, critical for DNA unwinding at the replicative fork during DNA replication. Overexpression or mutation in MCM2-7 genes is linked to and may drive several cancer types in humans. In mice, mutations in MCM2-7 genes result in growth retardation and mortality. All six MCM2-7 genes are also expressed in the developing mouse CNS, but their role in the CNS is not clear. Here, we use the central nervous system (CNS) of Drosophila melanogaster to begin addressing the role of the MCM complex during development, focusing on the specification of a well-studied neuropeptide expressing neuron: the Tv4/FMRFa neuron. In a search for genes involved in the specification of the Tv4/FMRFa neuron we identified Mcm5 and find that it plays a highly specific role in the specification of the Tv4/FMRFa neuron. We find that other components of the MCM2-7 complex phenocopies Mcm5, indicating that the role of Mcm5 in neuronal subtype specification involves the MCM2-7 complex. Surprisingly, we find no evidence of reduced progenitor proliferation, and instead find that Mcm5 is required for the expression of the type I BMP receptor Tkv, which is critical for the FMRFa expression. These results suggest that the MCM2-7 complex may play roles during CNS development outside of its well-established role during DNA replication. |
format | Online Article Text |
id | pubmed-9258838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92588382022-07-07 Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation Rubio-Ferrera, Irene Baladrón-de-Juan, Pablo Clarembaux-Badell, Luis Truchado-Garcia, Marta Jordán-Álvarez, Sheila Thor, Stefan Benito-Sipos, Jonathan Monedero Cobeta, Ignacio PLoS Genet Research Article The MCM2-7 complex is a highly conserved hetero-hexameric protein complex, critical for DNA unwinding at the replicative fork during DNA replication. Overexpression or mutation in MCM2-7 genes is linked to and may drive several cancer types in humans. In mice, mutations in MCM2-7 genes result in growth retardation and mortality. All six MCM2-7 genes are also expressed in the developing mouse CNS, but their role in the CNS is not clear. Here, we use the central nervous system (CNS) of Drosophila melanogaster to begin addressing the role of the MCM complex during development, focusing on the specification of a well-studied neuropeptide expressing neuron: the Tv4/FMRFa neuron. In a search for genes involved in the specification of the Tv4/FMRFa neuron we identified Mcm5 and find that it plays a highly specific role in the specification of the Tv4/FMRFa neuron. We find that other components of the MCM2-7 complex phenocopies Mcm5, indicating that the role of Mcm5 in neuronal subtype specification involves the MCM2-7 complex. Surprisingly, we find no evidence of reduced progenitor proliferation, and instead find that Mcm5 is required for the expression of the type I BMP receptor Tkv, which is critical for the FMRFa expression. These results suggest that the MCM2-7 complex may play roles during CNS development outside of its well-established role during DNA replication. Public Library of Science 2022-06-23 /pmc/articles/PMC9258838/ /pubmed/35737938 http://dx.doi.org/10.1371/journal.pgen.1010255 Text en © 2022 Rubio-Ferrera et al 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 the original author and source are credited. |
spellingShingle | Research Article Rubio-Ferrera, Irene Baladrón-de-Juan, Pablo Clarembaux-Badell, Luis Truchado-Garcia, Marta Jordán-Álvarez, Sheila Thor, Stefan Benito-Sipos, Jonathan Monedero Cobeta, Ignacio Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation |
title | Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation |
title_full | Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation |
title_fullStr | Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation |
title_full_unstemmed | Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation |
title_short | Selective role of the DNA helicase Mcm5 in BMP retrograde signaling during Drosophila neuronal differentiation |
title_sort | selective role of the dna helicase mcm5 in bmp retrograde signaling during drosophila neuronal differentiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258838/ https://www.ncbi.nlm.nih.gov/pubmed/35737938 http://dx.doi.org/10.1371/journal.pgen.1010255 |
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