𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Inhibition of methylation and changes in gene expression in relation to neural tube defects

✍ Scribed by Ivon J. M. van der Linden; Sandra G. Heil; Michael van Egmont Petersen; Henny W. van Straaten; Martin den Heijer; Henk J. Blom


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
148 KB
Volume
82
Category
Article
ISSN
1542-0752

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

BACKGROUND:

An impaired DNA methylation has been suggested to underlie the complex etiology of neural tube defects (NTDs). Previously, we have demonstrated that inhibition of methylation by periodate oxidized adenosine (Adox) results in a widening of the anterior neuropore (ANP) in our in vitro chick embryo model. Since DNA methylation is the chief regulator of gene expression, we hypothesize that inhibition of methylation by Adox in our in vitro chick embryo model will affect the expression of genes that may be involved in neurulation. In the present study, we therefore examined differential gene expression between Adox‐treated and control chick embryos, using the Affymetrix Genechip Chicken Genome Array.

METHODS:

Chick embryos of 4/5 somites were cultured in vitro with saline (control) or Adox and cranial parts were excised. Gene expression profiling was determined using the Affymetrix Genechip Chicken Genome Array on RNA isolated from two pools of Adox‐treated cranial parts (n = 12) and two pools of saline‐treated cranial parts (n = 12). Microarray data were validated by QPCR analysis.

RESULTS:

In the Adox‐treated chick embryos, 45 probesets were up‐regulated (fold ≥ 2.0, p < 0.05) and 32 probesets were down‐regulated (fold ≤ 0.5, p < 0.05). Of the 15 genes selected for QPCR analysis, the up‐regulation of phosphoserine phosphatase (PSPH), unc‐51‐like kinase 1 (ULK1), and chemokine (C‐X‐C motif) ligand 12/stromal cell‐derived factor 1 (CXCL12/SDF‐1) was confirmed.

CONCLUSIONS:

Inhibition of methylation by Adox affects gene expression in our in vitro chick embryo model. Further research will focus on the gene‐specific methylation patterns of PSPH, ULK1, and CXCL12/SDF‐1 and the role of the products of these genes in neurulation. Birth Defects Research (Part A) 82:676–683, 2008. © 2008 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Neurulation abnormalities secondary to a
✍ Bennett, Gregory D.; An, Jie; Craig, Johanna C.; Gefrides, Lisa A.; Calvin, Jame 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 133 KB 👁 2 views

The murine mutant Splotch (Sp) is a well-established model for studying neural tube closure defects. In the current investigation, the progression through neural tube closure (NTC) as well as the expression patterns of 12 developmentally regulated genes were examined in the neural tissue of wildtype

Identification of early-responsive genes
✍ Akinobu Okada; Kiyoshi Kushima; Yoshinobu Aoki; Meir Bialer; Michio Fujiwara 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 245 KB 👁 2 views

## BACKGROUND: Valproic acid (VPA) causes the failure of neural tube closure in newborn mice. However, the molecular mechanism of its teratogenesis is unknown. This study was conducted to investigate the genomewide effects of VPA disruption of normal neural tube development in mice. METHODS: Micro

Correlation of polymorphism of MTHFRs an
✍ Yali Shang; Hong Zhao; Bo Niu; Wan-I Li; Ran Zhou; Ting Zhang; Jun Xie 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 92 KB 👁 1 views

## Abstract ## BACKGROUND: Maternal periconceptional supplementation of folate reduces the incidence of neonatal Neural Tube Defects, indicating that changes in folate metabolism play a role in formation of NTDs. The mutations on two genes involved in folate metabolism, the __C677__ of the __MTHFR