Institute of Computing Technology, Chinese Academy IR
Single-cell Long Non-coding RNA Landscape of T Cells in Human Cancer Immunity | |
Luo, Haitao1,2,3; Bu, Dechao4; Shao, Lijuan1,2,3; Li, Yang5; Sun, Liang4; Wang, Ce1,2; Wang, Jing1,2,3; Yang, Wei1,2; Yang, Xiaofei1,2; Dong, Jun3; Zhao, Yi4; Li, Furong1,2 | |
2021-06-01 | |
发表期刊 | GENOMICS PROTEOMICS & BIOINFORMATICS |
ISSN | 1672-0229 |
卷号 | 19期号:3页码:377-393 |
摘要 | The development of new biomarkers or therapeutic targets for cancer immunotherapies requires deep understanding of T cells. To date, the complete landscape and systematic characterization of long noncoding RNAs (lncRNAs) in T cells in cancer immunity are lacking. Here, by systematically analyzing full-length single-cell RNA sequencing (scRNA-seq) data of more than 20,000 libraries of T cells across three cancer types, we provided the first comprehensive catalog and the functional repertoires of lncRNAs in human T cells. Specifically, we developed a custom pipeline for de novo transcriptome assembly and obtained a novel lncRNA catalog containing 9433 genes. This increased the number of current human lncRNA catalog by 16% and nearly doubled the number of lncRNAs expressed in T cells. We found that a portion of expressed genes in single T cells were lncRNAs which had been overlooked by the majority of previous studies. Based on metacell maps constructed by the MetaCell algorithm that partitions scRNA-seq datasets into disjointed and homogenous groups of cells (metacells), 154 signature lncRNA genes were identified. They were associated with effector, exhausted, and regulatory T cell states. Moreover, 84 of them were functionally annotated based on the co-expression networks, indicating that lncRNAs might broadly participate in the regulation of T cell functions. Our findings provide a new point of view and resource for investigating the mechanisms of T cell regulation in cancer immunity as well as for novel cancer-immune biomarker development and cancer immunotherapies. |
关键词 | Long non-coding RNA Transcriptome assembly Metacell Immune regulation Functional annotation |
DOI | 10.1016/j.gpb.2021.02.006 |
收录类别 | SCI |
语种 | 英语 |
资助项目 | Science and Technology Project of Shenzhen, China[JCYJ20190807145013281] ; Science and Technology Project of Shenzhen, China[JHZ20170310090257380] ; Science and Technology Project of Shenzhen, China[JCYJ20170413092711058] ; Science and Technology Project of Shenzhen, China[JCYJ20170307095822325] ; China Postdoctoral Science Foundation[2019M663369] ; National Natural Science Foundation of China[31970636] |
WOS研究方向 | Genetics & Heredity |
WOS类目 | Genetics & Heredity |
WOS记录号 | WOS:000753148400005 |
出版者 | ELSEVIER |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://119.78.100.204/handle/2XEOYT63/18999 |
专题 | 中国科学院计算技术研究所期刊论文_英文 |
通讯作者 | Luo, Haitao; Dong, Jun; Zhao, Yi; Li, Furong |
作者单位 | 1.Jinan Univ, Clin Med Coll 2, Shenzhen Peoples Hosp, Translat Med Collaborat Innovat Ctr, Shenzhen 518020, Peoples R China 2.Shenzhen Key Lab Stem Cell Res & Clin Transformat, Shenzhen 518020, Peoples R China 3.Jinan Univ, Integrated Chinese & Western Med Postdoctoral Res, Guangzhou 510632, Peoples R China 4.Chinese Acad Sci, Inst Comp Technol, Adv Comp Res Ctr, Key Lab Intelligent Informat Proc,Bioinformat Res, Beijing 100190, Peoples R China 5.Jinan Univ, Clin Med Coll 2, Shenzhen Peoples Hosp, Dept Gastrointestinal Surg, Shenzhen 518020, Peoples R China |
推荐引用方式 GB/T 7714 | Luo, Haitao,Bu, Dechao,Shao, Lijuan,et al. Single-cell Long Non-coding RNA Landscape of T Cells in Human Cancer Immunity[J]. GENOMICS PROTEOMICS & BIOINFORMATICS,2021,19(3):377-393. |
APA | Luo, Haitao.,Bu, Dechao.,Shao, Lijuan.,Li, Yang.,Sun, Liang.,...&Li, Furong.(2021).Single-cell Long Non-coding RNA Landscape of T Cells in Human Cancer Immunity.GENOMICS PROTEOMICS & BIOINFORMATICS,19(3),377-393. |
MLA | Luo, Haitao,et al."Single-cell Long Non-coding RNA Landscape of T Cells in Human Cancer Immunity".GENOMICS PROTEOMICS & BIOINFORMATICS 19.3(2021):377-393. |
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