科研之友
微信
新浪微博
Facebook
分享链接
摘要
Many genes exhibiting genomic Imprinting. parent-of-origin differences in gene expression, are involved in regulating placental and fetal growth. The goal of the present study was to assess whether abnormal regulation of Imprinted genes is associated with Intrauterine growth restriction (IUGR) and/or preeclampsia (PET)
Methods. Genomic DNA was extracted from at least two whole villi samples from control (N=22), IUGR (N = 13), PET (N = 17), and PET + IUGR (N = 21) placentas. Methylation was assessed using the Illumina GoldenGate Methylation Cancer Panel I array and Pyrosequencing and MS-SNuPE assays Results The 11p155 ICR1 (associated with H19 and IGF2) methylation showed considerable intra-placental variability Nonetheless, average methylation at this site was significantly decreased in normotensive IUGR placentas (p < 0.001). but not in any other group. Methylation at ICR2 (KvDMR1, associated with CDKN1C and other maternally expressed 11p15.5 genes) was not significantly altered in any group and no significant changes in expression levels were observed in the genes controlled by this region. There were no significant methylation changes observed in any candidate Imprinted gene evaluated by the Illumina array LINE-1 methylation, a marker of whole genome methylation, was also similar in all groups
Conclusions Reduced methylation of ICR1 is associated with normotensive IUGR but not IUGR associated with preeclampsia, suggesting a different etiology of IUGR in this group A reduction in placental IGF2 could be an adaptive response to restrict fetal growth in the presence of abnormal placentation or a response to poor fetal growth itself.
- 出版日期2010-3
