The histone replacement gene His4r is involved in heat stress induced chromatin rearrangement
His4r is the only known variant of histone H4 in Drosophila . It is encoded by the His4r single-copy gene that is located outside of the histone gene cluster and expressed in a different pattern than H4, although the encoded polypeptides are identical. We generated a null mutant ( His4r Δ42 ) which...
Gespeichert in:
Veröffentlicht in: | Scientific reports 2021-03, Vol.11 (1), p.4878-4878, Article 4878 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | His4r is the only known variant of histone H4 in
Drosophila
. It is encoded by the
His4r
single-copy gene that is located outside of the histone gene cluster and expressed in a different pattern than H4, although the encoded polypeptides are identical. We generated a null mutant (
His4r
Δ42
) which is homozygous viable and fertile without any apparent morphological defects. Heterozygous
His4r
Δ42
is a mild suppressor of position-effect variegation, suggesting that His4r has a role in the formation or maintenance of condensed chromatin. Under standard conditions loss of His4r has a modest effect on gene expression. Upon heat-stress the induction of the Heat shock protein (HSP) genes
Hsp27
and
Hsp68
is stronger in
His4r
Δ42
mutants with concordantly increased survival rate. Analysis of chromatin accessibility after heat shock at a
Hsp27
regulatory region showed less condensed chromatin in the absence of His4r while there was no difference at the gene body. Interestingly, preconditioning before heat shock led to increased chromatin accessibility, HSP gene transcription and survival rate in control flies while it did not cause notable changes in
His4r
Δ42
. Thus, our results suggest that His4r might play a role in fine tuning chromatin structure at inducible gene promoters upon environmental stress conditions. |
---|---|
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-021-84413-4 |