» Articles » PMID: 37165057

Identification of a Genomic DNA Sequence That Quantitatively Modulates KLF1 Transcription Factor Expression in Differentiating Human Hematopoietic Cells

Overview
Journal Sci Rep
Specialty Science
Date 2023 May 10
PMID 37165057
Authors
Affiliations
Soon will be listed here.
Abstract

The onset of erythropoiesis is under strict developmental control, with direct and indirect inputs influencing its derivation from the hematopoietic stem cell. A major regulator of this transition is KLF1/EKLF, a zinc finger transcription factor that plays a global role in all aspects of erythropoiesis. Here, we have identified a short, conserved enhancer element in KLF1 intron 1 that is important for establishing optimal levels of KLF1 in mouse and human cells. Chromatin accessibility of this site exhibits cell-type specificity and is under developmental control during the differentiation of human CD34+ cells towards the erythroid lineage. This site binds GATA1, SMAD1, TAL1, and ETV6. In vivo editing of this region in cell lines and primary cells reduces KLF1 expression quantitatively. However, we find that, similar to observations seen in pedigrees of families with KLF1 mutations, downstream effects are variable, suggesting that the global architecture of the site is buffered towards keeping the KLF1 genetic region in an active state. We propose that modification of intron 1 in both alleles is not equivalent to complete loss of function of one allele.

Citing Articles

Key Genes and under Acute High-Altitude Exposure: A Gene Expression and Network Analysis Based on Expression Profile Data.

Zhao Y, Zhu L, Shi D, Gao J, Fan M Genes (Basel). 2024; 15(8).

PMID: 39202434 PMC: 11353374. DOI: 10.3390/genes15081075.


Erythroid Krüppel-Like Factor (KLF1): A Surprisingly Versatile Regulator of Erythroid Differentiation.

Bieker J, Philipsen S Adv Exp Med Biol. 2024; 1459:217-242.

PMID: 39017846 DOI: 10.1007/978-3-031-62731-6_10.


Association of DDX5/p68 protein with the upstream erythroid enhancer element (EHS1) of the gene encoding the KLF1 transcription factor.

Chen X, Pillay S, Lohmann F, Bieker J J Biol Chem. 2023; 299(12):105489.

PMID: 38000658 PMC: 10750184. DOI: 10.1016/j.jbc.2023.105489.

References
1.
Stieglitz E, Taylor-Weiner A, Chang T, Gelston L, Wang Y, Mazor T . The genomic landscape of juvenile myelomonocytic leukemia. Nat Genet. 2015; 47(11):1326-1333. PMC: 4626387. DOI: 10.1038/ng.3400. View

2.
Zeng J, Wu Y, Ren C, Bonanno J, Shen A, Shea D . Therapeutic base editing of human hematopoietic stem cells. Nat Med. 2020; 26(4):535-541. PMC: 7869435. DOI: 10.1038/s41591-020-0790-y. View

3.
Liu Z, Liang J, Chen S, Wang K, Liu X, Liu B . Genome editing of CCR5 by AsCpf1 renders CD4T cells resistance to HIV-1 infection. Cell Biosci. 2020; 10:85. PMC: 7346486. DOI: 10.1186/s13578-020-00444-w. View

4.
Gnanapragasam M, McGrath K, Catherman S, Xue L, Palis J, Bieker J . EKLF/KLF1-regulated cell cycle exit is essential for erythroblast enucleation. Blood. 2016; 128(12):1631-41. PMC: 5034741. DOI: 10.1182/blood-2016-03-706671. View

5.
MILLER I, Bieker J . A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Krüppel family of nuclear proteins. Mol Cell Biol. 1993; 13(5):2776-86. PMC: 359658. DOI: 10.1128/mcb.13.5.2776-2786.1993. View