Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: KEGG:D02003 (
NBT
)
1,323
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Cell cycle progression is tightly regulated in hematopoietic stem cells. The cycle state decides cells' fates, which includes self-renewal, proliferation and differentiation. Proper cell cycle regulation is a pivotal element for the maintenance of hematopoiesis homeostasis.
HTm4
is a newly identified specific cell cycle regulator of the hematopoietic cell. Through interacting with KAP-CDK2 complex, it arrests cells in G(0)/G(1) phase. K562 is a human chronic myelogenous leukemia cell; it could be induced to megakaryoblast by phorbol 12-myristate 13-acetate (PMA). Such differentiation must be associated with cell cycle change. To further clarify
HTm4
's function in hematopoietic cell cycle regulation, K562 cells were treated with PMA. Cell cycle change was analysed using flow cytometric system. And during the induction process gene expression of
HTm4
as well as CycleE and CDK2, which are responsible for G(1) to S transition, were analysed using semi-quantitative RT-PCR. The C-terminal domain of
HTm4
protein has been shown to be important for
HTm4
's binding with KAP-CDK2 complex. To determine its impact on
HTm4
's function,
HTm4
and C-terminal truncated
HTm4
(HTm4-ct) were transfected into K562 cells using Tet-Off regulation expression system. Their influence on cell cycle was observed. The results showed that PMA induced both expansion and differentiation of K562 cells as measured by cell number count and
NBT
staining respectively. During PMA treatment, G(0)/G(1) cell proportion and
HTm4
expression displayed coordinated change, which suggested that
HTm4
might drive K562 cells out of cell cycle but was not involved in the quiescence maintenance. Additionally, transfection of
HTm4
caused G(0)/G(1) arrest in K562 cells, while transfection of
HTm4
-ct did not. It is therefore suggested that the C-terminal domain is important for the function of
HTm4
in cell cycle regulation.
...
PMID:[Regulatory role of HTm4 gene in hematopoietic cell cycle]. 1583 Jan 3