3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia

The non-coding genome of T-ALL has not been extensively studied. Here, the authors conduct RNA-seq, ATAC-seq and Hi-C seq analyses and find that T-ALL associated neo-loops may regulate key transcription factors including HOXA13; the aberrant expression of which is associated with poor prognosis.

Guardado en:
Detalles Bibliográficos
Autores principales: Lu Yang, Fengling Chen, Haichuan Zhu, Yang Chen, Bingjie Dong, Minglei Shi, Weitao Wang, Qian Jiang, Leping Zhang, Xiaojun Huang, Michael Q. Zhang, Hong Wu
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Q
Acceso en línea:https://doaj.org/article/ddc781751c044fe08a87e5cf4dd8d817
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ddc781751c044fe08a87e5cf4dd8d817
record_format dspace
spelling oai:doaj.org-article:ddc781751c044fe08a87e5cf4dd8d8172021-12-02T17:40:00Z3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia10.1038/s41467-021-24044-52041-1723https://doaj.org/article/ddc781751c044fe08a87e5cf4dd8d8172021-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-24044-5https://doaj.org/toc/2041-1723The non-coding genome of T-ALL has not been extensively studied. Here, the authors conduct RNA-seq, ATAC-seq and Hi-C seq analyses and find that T-ALL associated neo-loops may regulate key transcription factors including HOXA13; the aberrant expression of which is associated with poor prognosis.Lu YangFengling ChenHaichuan ZhuYang ChenBingjie DongMinglei ShiWeitao WangQian JiangLeping ZhangXiaojun HuangMichael Q. ZhangHong WuNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Lu Yang
Fengling Chen
Haichuan Zhu
Yang Chen
Bingjie Dong
Minglei Shi
Weitao Wang
Qian Jiang
Leping Zhang
Xiaojun Huang
Michael Q. Zhang
Hong Wu
3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia
description The non-coding genome of T-ALL has not been extensively studied. Here, the authors conduct RNA-seq, ATAC-seq and Hi-C seq analyses and find that T-ALL associated neo-loops may regulate key transcription factors including HOXA13; the aberrant expression of which is associated with poor prognosis.
format article
author Lu Yang
Fengling Chen
Haichuan Zhu
Yang Chen
Bingjie Dong
Minglei Shi
Weitao Wang
Qian Jiang
Leping Zhang
Xiaojun Huang
Michael Q. Zhang
Hong Wu
author_facet Lu Yang
Fengling Chen
Haichuan Zhu
Yang Chen
Bingjie Dong
Minglei Shi
Weitao Wang
Qian Jiang
Leping Zhang
Xiaojun Huang
Michael Q. Zhang
Hong Wu
author_sort Lu Yang
title 3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia
title_short 3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia
title_full 3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia
title_fullStr 3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia
title_full_unstemmed 3D genome alterations associated with dysregulated HOXA13 expression in high-risk T-lineage acute lymphoblastic leukemia
title_sort 3d genome alterations associated with dysregulated hoxa13 expression in high-risk t-lineage acute lymphoblastic leukemia
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/ddc781751c044fe08a87e5cf4dd8d817
work_keys_str_mv AT luyang 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT fenglingchen 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT haichuanzhu 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT yangchen 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT bingjiedong 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT mingleishi 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT weitaowang 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT qianjiang 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT lepingzhang 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT xiaojunhuang 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT michaelqzhang 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
AT hongwu 3dgenomealterationsassociatedwithdysregulatedhoxa13expressioninhighrisktlineageacutelymphoblasticleukemia
_version_ 1718379795331416064