Identification of region-specific gene isoforms in the human brain using long-read transcriptome sequencing

被引:6
|
作者
Shimada, Mihoko [1 ,2 ,3 ]
Omae, Yosuke [1 ]
Kakita, Akiyoshi [4 ]
Gabdulkhaev, Ramil [4 ]
Hitomi, Yuki [5 ]
Miyagawa, Taku [3 ]
Honda, Makoto [3 ,6 ,7 ]
Fujimoto, Akihiro [8 ]
Tokunaga, Katsushi [1 ]
机构
[1] Natl Ctr Global Hlth & Med NCGM, Genome Med Sci Project Toyama, Tokyo, Japan
[2] Natl Ctr Global Hlth & Med NCGM, Ctr Clin Sci, Tokyo, Japan
[3] Tokyo Metropolitan Inst Med Sci, Dept Psychiat & Behav Sci, Sleep Disorders Project, Tokyo, Japan
[4] Niigata Univ, Brain Res Inst, Dept Pathol, Niigata, Japan
[5] Natl Ctr Global Hlth & Med NCGM, Res Inst, Dept Human Genet, Tokyo, Japan
[6] Japan Somnol Ctr, Tokyo, Japan
[7] Seiwa Hosp, Inst Neuropsychiat, Tokyo, Japan
[8] Univ Tokyo, Grad Sch Med, Dept Human Genet, Tokyo, Japan
关键词
INTRAGENIC DNA METHYLATION; BODY-SPECIFIC METHYLATION; EXPRESSION; GAS7; ORGANIZATION; GROWTH;
D O I
10.1126/sciadv.adj5279
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In neurological and neuropsychiatric diseases, different brain regions are affected, and differences in gene expression patterns could potentially explain this mechanism. However, limited studies have precisely explored gene expression in different regions of the human brain. In this study, we performed long-read RNA sequencing on three different brain regions of the same individuals: the cerebellum, hypothalamus, and temporal cortex. Despite stringent filtering criteria excluding isoforms predicted to be artifacts, over half of the isoforms expressed in multiple samples across multiple regions were found to be unregistered in the GENCODE reference. We then especially focused on genes with different major isoforms in each brain region, even with similar overall expression levels, and identified that many of such genes including GAS7 might have distinct roles in dendritic spine and neuronal formation in each region. We also found that DNA methylation might, in part, drive different isoform expressions in different regions. These findings highlight the significance of analyzing isoforms expressed in disease-relevant sites.
引用
收藏
页数:15
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