转座因子在正常和白血病造血中形成干细胞。

IF 29 1区 生物学 Q1 GENETICS & HEREDITY
Giacomo Grillo, Bettina Nadorp, Aditi Qamra, Bryce Drylie, Amanda Mitchell, Christopher Arlidge, Ankita Nand, Naoya Takayama, Alex Murison, Seyed Ali Madani Tonekaboni, Komaldeep Kaur Kang, Andrea Arruda, Jean C Y Wang, Mark D Minden, Özgen Deniz, Héléna Boutzen, John E Dick, Mathieu Lupien
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引用次数: 0

摘要

尽管大多数急性髓性白血病(AML)患者在诱导化疗后达到完全缓解,但三分之二的患者在5年内复发。AML遵循由白血病干细胞(LSCs)维持的细胞层次结构,其驱动肿瘤进展和复发。我们对驱动LSCs干细胞特性的遗传决定因素知之甚少。通过从LSCs、造血干细胞和下游后代的可及性测量中鉴定染色质变异,我们确定了转座因子(te)是原始群体与成熟群体的遗传决定因素。121个TE亚家族的可及性通过干细胞和存活率将LSCs与成熟白血病细胞和分层AML患者区分开来。功能分析显示,这些TE亚家族充当基因组拓扑调节因子或谱系特异性转录因子(包括LSCs中的LYL1)的对接位点。染色质编辑确定了LTR12C元件可及性的必要性,以维持LSC的干系性。因此,TEs调节原始和成熟细胞状态,在正常和白血病干细胞中具有不同的亚家族。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transposable elements shape stemness in normal and leukemic hematopoiesis.

Despite most acute myeloid leukemia (AML) patients achieving complete remission after induction chemotherapy, two-thirds relapse within 5 years. AML follows a cellular hierarchy sustained by leukemia stem cells (LSCs), which drive tumor progression and relapse. Little is known about the genetic determinants driving LSCs stemness properties. By identifying chromatin variants from accessibility measurements across LSCs, hematopoietic stem cells and downstream progeny, we identified transposable elements (TEs) as genetic determinants of primitive versus mature populations. Accessibility at 121 TE subfamilies distinguished LSCs from mature leukemic cells and stratified AML patients by stemness and survival. Functional assays revealed that these TE subfamilies serve as docking sites for genome topology regulators or lineage-specific transcription factors, including LYL1 in LSCs. Chromatin editing established the necessity of accessibility at LTR12C elements to maintain LSC stemness. Thus, TEs regulate primitive versus mature cell states, with distinct subfamilies underlying stemness in normal versus leukemic stem cells.

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来源期刊
Nature genetics
Nature genetics 生物-遗传学
CiteScore
43.00
自引率
2.60%
发文量
241
审稿时长
3 months
期刊介绍: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution
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