Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes

Topoisomerase I is required for the proper expression of long genes (>100 kb) in mouse and human cortical neurons, including many candidate genes for autism spectrum disorder (ASD) [1]. Given the important role of astrocytes in brain development [2], we investigated whether long genes, including...

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Main Authors: Akira Gokoolparsadh, Zhiming Fang, Nady Braidy, Irina Voineagu
Format: Article
Language:English
Published: Elsevier 2017-03-01
Series:Genomics Data
Online Access:http://www.sciencedirect.com/science/article/pii/S2213596016301805
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spelling doaj-7eac19306e4c4643b5f836d832826f502020-11-25T01:41:14ZengElsevierGenomics Data2213-59602017-03-0111C11311510.1016/j.gdata.2016.12.005Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytesAkira Gokoolparsadh0Zhiming Fang1Nady Braidy2Irina Voineagu3School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, AustraliaSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, AustraliaCentre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, AustraliaSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, AustraliaTopoisomerase I is required for the proper expression of long genes (>100 kb) in mouse and human cortical neurons, including many candidate genes for autism spectrum disorder (ASD) [1]. Given the important role of astrocytes in brain development [2], we investigated whether long genes, including autism susceptibility genes, also require topoisomerase I expression in human primary astrocytes. We carried genome-wide expression profiling of cultured human primary astrocytes following treatment with the topoisomerase I inhibitor Topotecan, using Illumina microarrays. We identified several thousands of differentially expressed genes and confirmed that topoisomerase I inhibition affects gene expression in human primary astrocytes in a length-dependent manner. We also identified over 20 ASD-associated genes that show topoisomerase-dependent gene expression in human primary astrocytes but have not been previously reported as topoisomerase-I-dependent in neurons. The microarray data have been deposited in NCBI GEO (https://www.ncbi.nlm.nih.gov/geo/) under accession number GSE90052.http://www.sciencedirect.com/science/article/pii/S2213596016301805
collection DOAJ
language English
format Article
sources DOAJ
author Akira Gokoolparsadh
Zhiming Fang
Nady Braidy
Irina Voineagu
spellingShingle Akira Gokoolparsadh
Zhiming Fang
Nady Braidy
Irina Voineagu
Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
Genomics Data
author_facet Akira Gokoolparsadh
Zhiming Fang
Nady Braidy
Irina Voineagu
author_sort Akira Gokoolparsadh
title Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
title_short Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
title_full Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
title_fullStr Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
title_full_unstemmed Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
title_sort topoisomerase i inhibition leads to length-dependent gene expression changes in human primary astrocytes
publisher Elsevier
series Genomics Data
issn 2213-5960
publishDate 2017-03-01
description Topoisomerase I is required for the proper expression of long genes (>100 kb) in mouse and human cortical neurons, including many candidate genes for autism spectrum disorder (ASD) [1]. Given the important role of astrocytes in brain development [2], we investigated whether long genes, including autism susceptibility genes, also require topoisomerase I expression in human primary astrocytes. We carried genome-wide expression profiling of cultured human primary astrocytes following treatment with the topoisomerase I inhibitor Topotecan, using Illumina microarrays. We identified several thousands of differentially expressed genes and confirmed that topoisomerase I inhibition affects gene expression in human primary astrocytes in a length-dependent manner. We also identified over 20 ASD-associated genes that show topoisomerase-dependent gene expression in human primary astrocytes but have not been previously reported as topoisomerase-I-dependent in neurons. The microarray data have been deposited in NCBI GEO (https://www.ncbi.nlm.nih.gov/geo/) under accession number GSE90052.
url http://www.sciencedirect.com/science/article/pii/S2213596016301805
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AT zhimingfang topoisomeraseiinhibitionleadstolengthdependentgeneexpressionchangesinhumanprimaryastrocytes
AT nadybraidy topoisomeraseiinhibitionleadstolengthdependentgeneexpressionchangesinhumanprimaryastrocytes
AT irinavoineagu topoisomeraseiinhibitionleadstolengthdependentgeneexpressionchangesinhumanprimaryastrocytes
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