Genome-wide association study on 13 167 individuals identifies regulators of blood CD34+ cell levels

Stem cell transplantation is a cornerstone in the treatment of blood malignancies. The most common method to harvest stem cells for transplantation is by leukapheresis, requiring mobilization of CD341 hematopoietic stem and progenitor cells (HSPCs) from the bone marrow into the blood. Identifying the genetic factors that control blood CD341 cell levels could reveal new drug targets for HSPC mobilization. Here we report the first large-scale, genome-wide association study on blood CD341 cell levels. Across 13167 individuals, we identify 9 significant and 2 suggestive associations, accounted for by 8 loci (PPM1H, CXCR4, ENO1-RERE, ITGA9, ARHGAP45, CEBPA, TERT, and MYC). Notably, 4 of the identified associations map to CXCR4, showing that bona fide regulators of blood CD341 cell levels can be identified through genetic variation. Further, the most significant association maps to PPM1H, encoding a serine/threonine phosphatase never previously implicated in HSPC biology. PPM1H is expressed in HSPCs, and the allele that confers higher blood CD341 cell levels downregulates PPM1H. Through functional fine-mapping, we find that this downregulation is caused by the variant rs772557-A, which abrogates an MYB transcription factor-binding site in PPM1H intron 1 that is active in specific HSPC subpopulations, including hematopoietic stem cells, and interacts with the promoter by chromatin looping. Furthermore, PPM1H knockdown increases the proportion of CD341 and CD341901 cells in cord blood assays. Our results provide the first large-scale analysis of the genetic architecture of blood CD341 cell levels and warrant further investigation of PPM1H as a potential inhibition target for stem cell mobilization.

Automated summary

This study provides the first large-scale analysis of the genetic architecture of blood CD341 cell levels, identifying several associated loci including PPM1H and CXCR4. Functional fine-mapping suggests that the downregulation of PPM1H may be mediated through the regulation of MYB transcription factor binding site. These results warrant further investigation of PPM1H as a potential inhibition target for stem cell mobilization.