Acetylation of hepatic histone H3 in rats with intrauterine growth retardation.
- Author:
Xiao-Mei LIU
1
;
Hai-Lan ZHANG
;
Wei-Wei SONG
;
Yi-Sheng JIAO
;
Yan LU
Author Information
- Publication Type:Journal Article
- MeSH: Acetylation; Animals; Female; Fetal Growth Retardation; metabolism; Histone Deacetylase 1; analysis; genetics; Histones; metabolism; Liver; metabolism; Male; Pregnancy; RNA, Messenger; analysis; Rats; Rats, Wistar
- From: Chinese Journal of Contemporary Pediatrics 2009;11(9):753-756
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effects of intrauterine growth retardation (IUGR) caused by malnutrition during pregnancy on the acetylation of histone H3 and expression of histonedeacetylase1(HDAC1) in the hepar of the adult offspring and to explore the relationship between them.
METHODSMale 8-week-old offspring from maternal protein-malnutrition dams were studied. The expression of HDAC1 mRNA in the hepar was measured by fluorescent quantization RT-PCR. The levels of hepatic nuclear HDAC1 protein and acetylation of histone H3/K9 were assessed by Western blot.
RESULTSThe hepatic HDAC1 mRNA expression in IUGR rats was reduced to 54% of that of normal control rats (t=2.042, p<0.05). A decline in nuclear expression of HDAC1 protein (438 +/- 47) was also noted when compared with normal controls (1,128 +/- 110) (t=2.179, p<0.05). In contrast, the percentage of acetylated histone H3/K9 in IUGR rats (17.3 +/- 1.6%) increased significantly compared with that of normal control rats (10.5 +/- 1.2%) (t=3.597, p<0.01). The level of acetylated histone H3/K9 was negatively correlated with the HDAC1 protein concentration (r=-0.781, p<0.01).
CONCLUSIONSIncreased hepatic acetylation of histone H3 in the IUGR offspring might be caused by decreased HDAC1 expression in nuclear protein. This may contribute to the transcription change of some genes in the hepar.