拓扑异构酶I抑制导致人原代星形胶质细胞长度依赖性基因表达变化

Akira Gokoolparsadh , Zhiming Fang , Nady Braidy , Irina Voineagu
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引用次数: 5

摘要

拓扑异构酶I是长基因正确表达所必需的。100kb),包括许多自闭症谱系障碍(ASD)[1]的候选基因。鉴于星形胶质细胞在脑发育中的重要作用,我们研究了长基因,包括自闭症易感基因,是否也需要在人类初级星形胶质细胞中表达拓扑异构酶I。我们使用Illumina微阵列对经拓扑异构酶I抑制剂Topotecan处理的培养人原代星形胶质细胞进行了全基因组表达谱分析。我们鉴定了数千个差异表达基因,并证实拓扑异构酶I抑制以长度依赖的方式影响人类原代星形胶质细胞的基因表达。我们还发现了20多个asd相关基因,这些基因在人类原代星形胶质细胞中显示拓扑异构酶依赖性基因表达,但在神经元中尚未报道拓扑异构酶依赖性基因表达。微阵列数据已存入NCBI GEO (https://www.ncbi.nlm.nih.gov/geo/),登录号为GSE90052。
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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 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.

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