Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets

A subset of expressed genes is associated with a broad H3K4me3 (histone H3 trimethylated at lysine 4) domain that extends throughout the gene body. Genes marked in this way in normal cells are involved in cell-identity and tumor-suppressor activities, whereas in cancer cells, genes driving the cance...

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Main Authors: Prerna Sharma, Hedieh Sattarifard, Narges Fatemiyan, Ted M. Lakowski, James R. Davie
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/18/2830
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author Prerna Sharma
Hedieh Sattarifard
Narges Fatemiyan
Ted M. Lakowski
James R. Davie
author_facet Prerna Sharma
Hedieh Sattarifard
Narges Fatemiyan
Ted M. Lakowski
James R. Davie
author_sort Prerna Sharma
collection DOAJ
description A subset of expressed genes is associated with a broad H3K4me3 (histone H3 trimethylated at lysine 4) domain that extends throughout the gene body. Genes marked in this way in normal cells are involved in cell-identity and tumor-suppressor activities, whereas in cancer cells, genes driving the cancer phenotype (oncogenes) have this feature. Other histone modifications associated with expressed genes that display a broad domain have been less studied. Here, we identified genes with the broadest H3K79me2 (histone H3 dimethylated at lysine 79) domain in human leukemic cell lines representing different forms of leukemia. Taking a bioinformatic approach, we provide evidence that genes with the broadest H3K79me2 domain have known roles in leukemia (e.g., <i>JMJD1C</i>). In the mixed-lineage leukemia cell line MOLM-13, the <i>HOXA9</i> gene is in a 100 kb broad H3K79me2 domain with other <i>HOXA</i> protein-coding and oncogenic long non-coding RNA genes. The genes in this domain contribute to leukemia. This broad H3K79me2 domain has an unstable chromatin structure, as was evident by enhanced chromatin accessibility throughout. Together, we provide evidence that identification of genes with the broadest H3K79me2 domain will aid in generating a panel of genes in the diagnosis and therapeutic treatment of leukemia in the future.
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spelling doaj.art-d7625b9e31ab4725b4f8683e38ee79192023-11-23T15:32:57ZengMDPI AGCells2073-44092022-09-011118283010.3390/cells11182830Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data SetsPrerna Sharma0Hedieh Sattarifard1Narges Fatemiyan2Ted M. Lakowski3James R. Davie4Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E 0J9, CanadaDepartment of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E 0J9, CanadaDepartment of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E 0J9, CanadaCollege of Pharmacy Pharmaceutical Analysis Laboratory, University of Manitoba, Winnipeg, MB R3E 0V9, CanadaDepartment of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E 0J9, CanadaA subset of expressed genes is associated with a broad H3K4me3 (histone H3 trimethylated at lysine 4) domain that extends throughout the gene body. Genes marked in this way in normal cells are involved in cell-identity and tumor-suppressor activities, whereas in cancer cells, genes driving the cancer phenotype (oncogenes) have this feature. Other histone modifications associated with expressed genes that display a broad domain have been less studied. Here, we identified genes with the broadest H3K79me2 (histone H3 dimethylated at lysine 79) domain in human leukemic cell lines representing different forms of leukemia. Taking a bioinformatic approach, we provide evidence that genes with the broadest H3K79me2 domain have known roles in leukemia (e.g., <i>JMJD1C</i>). In the mixed-lineage leukemia cell line MOLM-13, the <i>HOXA9</i> gene is in a 100 kb broad H3K79me2 domain with other <i>HOXA</i> protein-coding and oncogenic long non-coding RNA genes. The genes in this domain contribute to leukemia. This broad H3K79me2 domain has an unstable chromatin structure, as was evident by enhanced chromatin accessibility throughout. Together, we provide evidence that identification of genes with the broadest H3K79me2 domain will aid in generating a panel of genes in the diagnosis and therapeutic treatment of leukemia in the future.https://www.mdpi.com/2073-4409/11/18/2830leukemiabroad H3K79me2 domainsDOT1Lepigeneticschromatin accessibility
spellingShingle Prerna Sharma
Hedieh Sattarifard
Narges Fatemiyan
Ted M. Lakowski
James R. Davie
Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets
Cells
leukemia
broad H3K79me2 domains
DOT1L
epigenetics
chromatin accessibility
title Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets
title_full Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets
title_fullStr Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets
title_full_unstemmed Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets
title_short Bioinformatic Analyses of Broad H3K79me2 Domains in Different Leukemia Cell Line Data Sets
title_sort bioinformatic analyses of broad h3k79me2 domains in different leukemia cell line data sets
topic leukemia
broad H3K79me2 domains
DOT1L
epigenetics
chromatin accessibility
url https://www.mdpi.com/2073-4409/11/18/2830
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