Abstract
Tematopoietic stem cells provide life-long production of blood cells and undergo self-renewal division in order to sustain the stem cell pool. Homeostatic maintenance of hematopoietic stem cell pool and blood cell production is vital for the organism to survive. We previously reported that latexin is a negative regulator of hematopoietic stem cells in mice. Its natural variation in the expression is inversely correlated with hematopoietic stem cell number. However, the molecular mechanisms regulating latexin transcription remain largely unknown, and the genetic factors contributing to its natural variation are not clearly defined. Here we discovered a chromatin protein, high-mobility group protein B2, as a novel transcriptional suppressor of latexin by using DNA pull-down and mass spectrometry. High-mobility group protein B2 knockdown increases latexin expression at transcript and protein levels, and decreases hematopoietic stem cell number and regeneration capacity in vivo. Concomitant blockage of latexin activation significantly reverses these phenotypic changes, suggesting that latexin is one of the downstream targets and functional mediators of high-mobility group protein B2. We further identified a functional single nucleotide polymorphism, rs31528793, in the latexin promoter that binds to high-mobility group protein B2 and affects the promoter activity. G allelic variation in rs31528793 associates with the higher latexin expression and lower hematopoietic stem cell number, whereas C allele indicates the lower latexin expression and higher stem cell number. This study reveals for the first time that latexin transcription is regulated by both transacting (high-mobility group protein B2) and cis-acting (single nucleotide polymorphism rs31528793) factors. It uncovers the functional role of naturally occurring genetic variants, in combination with epigenetic regulator, in determining differential gene expression and phenotypic diversity in the hematopoietic stem cell population.
| Original language | English |
|---|---|
| Pages (from-to) | 573-584 |
| Number of pages | 12 |
| Journal | Haematologica |
| Volume | 105 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 1 2020 |
Bibliographical note
Funding Information:The authors are supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health under awards R01HL124015(YL), R21HL140213 (YL), UKY-CCTS UL1TR001998 (UKY-CCTS pilot), and the Markey Cancer Center’s Biostatistics and Bioinformatics Shared Resource Facility as well as the Flow Cytometry Shared Resource Facility (P30CA177558). We thank the Markey Cancer Center's Research Communications Office for editing and graphics support.
Funding Information:
The authors are supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health under awards R01HL124015(YL), R21HL140213 (YL), UKY-CCTS UL1TR001998 (UKY-CCTS pilot), and the Markey Cancer Center?s Biostatistics and Bioinformatics Shared Resource Facility as well as the Flow Cytometry Shared Resource Facility (P30CA177558). We thank the Markey Cancer Center's Research Communications Office for editing and graphics support.
Publisher Copyright:
©2020 Ferrata Storti Foundation
ASJC Scopus subject areas
- Hematology