Macrophages and their precursor cells, monocytes, are the first line of defense of the body against foreign pathogens and tissue damage. Although the origins of macrophages are diverse, some common transcription factors (such as PU.1) are required to ensure proper development of monocytes/macrophages. Here, we report that the deficiency of zbtb14 , a transcription repressor gene belonging to ZBTB family, leads to an aberrant expansion of monocyte/macrophage population in zebrafish. Mechanistically, Zbtb14 functions as a negative regulator of pu.1 , and SUMOylation on a conserved lysine is essential for the repression activity of Zbtb14. Moreover, a serine to phenylalanine mutation found in an acute myeloid leukemia (AML) patient could target ZBTB14 protein to autophagic degradation. Hence, ZBTB14 is a newly identified gene implicated in both normal and malignant myelopoiesis.
Keyphrases
- acute myeloid leukemia
- transcription factor
- dendritic cells
- peripheral blood
- adipose tissue
- cell death
- genome wide identification
- induced apoptosis
- endothelial cells
- copy number
- signaling pathway
- oxidative stress
- cell cycle arrest
- gene expression
- case report
- immune response
- dna methylation
- acute lymphoblastic leukemia
- antimicrobial resistance
- smoking cessation
- dna binding