TABLE 1.
Alterations and functions of hub genes during HSC the aging process.
Gene | Aliase | Alterations with age | Functions |
---|---|---|---|
Aurka | Aurora kinase A | Down | Contributed to the regulation of cell cycle progression |
Ccna2 | Cyclin-A2 | Down | Controlled both the G1/S and the G2/M transition phases of the cell cycle |
Ccnb2 | G2/mitotic-specific cyclin-B2 | Down | Essential for the control of the cell cycle at the G2/M transition |
Cdk1 | Cyclin-dependent kinase 1 | Down | Essential for the control of the eukaryotic cell cycle, promoted G2-M transition, and regulated G1 progress and G1-S transition |
Birc5 | Baculoviral IAP repeat-containing protein 5 | Down | Had dual roles in promoting cell proliferation and preventing apoptosis |
Jun | Transcription factor AP-1 | Up | Regulated functional development of hematopoietic precursor cells into mature blood cells |
Aldh1a1 | Retinal dehydrogenase 1 | Up | Regulated retinoic acid biosynthesis, the clearance of toxic byproducts of reactive oxygen species and HSC differentiation |
Egr1 | Early growth response protein 1 | Up | Played a role in the regulation of cell survival, proliferation and cell death and in regulating the response to growth factors and DNA damage |
Cd38 | Cluster of Differentiation 38 | Up | Cell adhesion and signal transduction |
Junb | Transcription factor jun-B | Up | Involved in regulating gene activity following the primary growth factor response |