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Topoisomerases facilitate transcription of long genes linked to autism

Topoisomerases are expressed throughout the developing and adult brain and are mutated in some individuals with autism spectrum disorder (ASD). However, how topoisomerases are mechanistically connected to ASD is unknown. Here we found that topotecan, a Topoisomerase 1 (TOP1) inhibitor, dose-dependen...

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Autores principales: King, Ian F., Yandava, Chandri N., Mabb, Angela M., Hsiao, Jack S., Huang, Hsien-Sung, Pearson, Brandon L., Calabrese, J. Mauro, Starmer, Joshua, Parker, Joel S., Magnuson, Terry, Chamberlain, Stormy J., Philpot, Benjamin D., Zylka, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767287/
https://www.ncbi.nlm.nih.gov/pubmed/23995680
http://dx.doi.org/10.1038/nature12504
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author King, Ian F.
Yandava, Chandri N.
Mabb, Angela M.
Hsiao, Jack S.
Huang, Hsien-Sung
Pearson, Brandon L.
Calabrese, J. Mauro
Starmer, Joshua
Parker, Joel S.
Magnuson, Terry
Chamberlain, Stormy J.
Philpot, Benjamin D.
Zylka, Mark J.
author_facet King, Ian F.
Yandava, Chandri N.
Mabb, Angela M.
Hsiao, Jack S.
Huang, Hsien-Sung
Pearson, Brandon L.
Calabrese, J. Mauro
Starmer, Joshua
Parker, Joel S.
Magnuson, Terry
Chamberlain, Stormy J.
Philpot, Benjamin D.
Zylka, Mark J.
author_sort King, Ian F.
collection PubMed
description Topoisomerases are expressed throughout the developing and adult brain and are mutated in some individuals with autism spectrum disorder (ASD). However, how topoisomerases are mechanistically connected to ASD is unknown. Here we found that topotecan, a Topoisomerase 1 (TOP1) inhibitor, dose-dependently reduced the expression of extremely long genes in mouse and human neurons, including nearly all genes >200 kb. Expression of long genes was also reduced following knockdown of Top1 or Top2b in neurons, highlighting that each enzyme was required for full expression of long genes. By mapping RNA polymerase II density genome-wide in neurons, we found that this length-dependent effect on gene expression was due to impaired transcription elongation. Interestingly, many high confidence ASD candidate genes are exceptionally long and were reduced in expression following TOP1 inhibition. Our findings suggest that chemicals and genetic mutations that impair topoisomerases could commonly contribute to ASD and other neurodevelopmental disorders.
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spelling pubmed-37672872014-03-05 Topoisomerases facilitate transcription of long genes linked to autism King, Ian F. Yandava, Chandri N. Mabb, Angela M. Hsiao, Jack S. Huang, Hsien-Sung Pearson, Brandon L. Calabrese, J. Mauro Starmer, Joshua Parker, Joel S. Magnuson, Terry Chamberlain, Stormy J. Philpot, Benjamin D. Zylka, Mark J. Nature Article Topoisomerases are expressed throughout the developing and adult brain and are mutated in some individuals with autism spectrum disorder (ASD). However, how topoisomerases are mechanistically connected to ASD is unknown. Here we found that topotecan, a Topoisomerase 1 (TOP1) inhibitor, dose-dependently reduced the expression of extremely long genes in mouse and human neurons, including nearly all genes >200 kb. Expression of long genes was also reduced following knockdown of Top1 or Top2b in neurons, highlighting that each enzyme was required for full expression of long genes. By mapping RNA polymerase II density genome-wide in neurons, we found that this length-dependent effect on gene expression was due to impaired transcription elongation. Interestingly, many high confidence ASD candidate genes are exceptionally long and were reduced in expression following TOP1 inhibition. Our findings suggest that chemicals and genetic mutations that impair topoisomerases could commonly contribute to ASD and other neurodevelopmental disorders. 2013-08-28 2013-09-05 /pmc/articles/PMC3767287/ /pubmed/23995680 http://dx.doi.org/10.1038/nature12504 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
King, Ian F.
Yandava, Chandri N.
Mabb, Angela M.
Hsiao, Jack S.
Huang, Hsien-Sung
Pearson, Brandon L.
Calabrese, J. Mauro
Starmer, Joshua
Parker, Joel S.
Magnuson, Terry
Chamberlain, Stormy J.
Philpot, Benjamin D.
Zylka, Mark J.
Topoisomerases facilitate transcription of long genes linked to autism
title Topoisomerases facilitate transcription of long genes linked to autism
title_full Topoisomerases facilitate transcription of long genes linked to autism
title_fullStr Topoisomerases facilitate transcription of long genes linked to autism
title_full_unstemmed Topoisomerases facilitate transcription of long genes linked to autism
title_short Topoisomerases facilitate transcription of long genes linked to autism
title_sort topoisomerases facilitate transcription of long genes linked to autism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767287/
https://www.ncbi.nlm.nih.gov/pubmed/23995680
http://dx.doi.org/10.1038/nature12504
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