Grass carp (Ctenopharyngodon idella) Bcl-xl: transcriptional regulation and anti-apoptosis analysis
Bcl-xl, Bax2, and NF-κB are well-known to be involved in anti-apoptosis response. Although Bcl-xl has been reported in fish, the NF-κB-mediated regulatory mechanism and anti-apoptotic function are still unclear. Here, we cloned and characterized the full-length cDNA sequence of grass carp ( Ctenopha...
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Veröffentlicht in: | Fish physiology and biochemistry 2020-04, Vol.46 (2), p.483-500 |
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Zusammenfassung: | Bcl-xl, Bax2, and NF-κB are well-known to be involved in anti-apoptosis response. Although Bcl-xl has been reported in fish, the NF-κB-mediated regulatory mechanism and anti-apoptotic function are still unclear. Here, we cloned and characterized the full-length cDNA sequence of grass carp (
Ctenopharyngodon idella
) Bcl-xl (
CiBcl-xl
) and its promoter region sequence. The full-length cDNA of
CiBcl-xl
is 2836 bp with an ORF of 627 bp encoding a polypeptide of 208 amino acids. Phylogenetic tree analysis revealed that
CiBcl-xl
shared high homology with
Dario rerio
Bcl-xl (
DrBcl-xl
). After stimulation with Poly I:C, the expression of
CiBcl-xl
in CIK cells and various tested tissues of grass carp were significantly upregulated. To further understand the transcriptional control of fish
Bcl-xl
induced by NF-κB,
CiC-rel
and
Cip65
were expressed in
Escherichia coli
BL21 and purified by affinity chromatography with the Ni-NTA His-Bind resin. In vitro, gel mobility shift assays demonstrated the high affinity of
Ci
C-rel and
Ci
p65 with
CiBcl-xl
promoter. Dual-luciferase reporter assays showed that
Ci
C-rel and
Ci
p65 activated
CiBcl-xl
promoter. Also, knockdown of
Ci
C-rel and
Ci
p65 reduced the expression of
Bcl-xl
. Therefore, similar to those of mammals, fish C-rel and p65 can upregulate the transcription of
Bcl-xl
. In addition, we found that overexpression of
Ci
Bcl-xl in CIK cells increased the cell activity and inhibited cell apoptosis, while overexpression of Bax2 promoted cell apoptosis. Meanwhile, co-transfection of
CiBcl-xl
and
CiBax2
into cells can ease up apoptotic rate. To further investigate the molecular basis of synergistic effect of Bcl-xl and Bax2, we showed that Bcl-xl and Bax2 interacted with each other. The results suggested that Bcl-xl executed its anti-apoptotic function by binding to and inhibiting the pro-apoptotic activity of Bax2. |
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ISSN: | 0920-1742 1573-5168 |
DOI: | 10.1007/s10695-019-00668-9 |