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Neural tube development requires the cooperation of p53- and Gadd45a-associated pathways

✍ Scribed by Andrew D. Patterson; Jeffrey Hildesheim; Albert J. Fornace Jr.; M. Christine Hollander


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
95 KB
Volume
76
Category
Article
ISSN
1542-0752

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✦ Synopsis


Abstract

BACKGROUND

Numerous genetically engineered mouse models for neural tube defects (NTDs) exist, and some of the implicated proteins are functionally related. For example, the growth arrest and DNA damage‐inducible protein Gadd45a and tumor suppressor p53 are functionally similar, and both are involved in neural tube development (Gadd45a‐ and Trp53‐null embryos show low levels of exencephaly). To assess their roles in neural tube development, we generated double‐null mice from Gadd45a‐ and Trp53‐null mice, as well as from cyclin‐dependent kinase inhibitor (Cdkn1a) (p21)‐null and xeroderma pigmentosum group C (XPC)‐null mice that do not show spontaneous exencephaly.

METHODS

Gadd45a‐, Trp53‐, Cdkn1a‐, and XPC‐null mice were crossed to generate several double‐null mouse models. Embryos (embryonic day [ED] 16–18) from the single‐ and double‐null crosses were scored for NTDs.

RESULTS

Deletion of both Gadd45a and Trp53 in mice increased exencephaly frequencies compared to the deletion of either single gene (34.0% in Gadd45a/Trp53‐null compared to 8.4% and 9.1% in the Gadd45a‐ and Trp53‐null embryos, respectively). Furthermore, although deletion of another p53‐regulated gene, Cdkn1a, is not associated with exencephaly, in conjunction with Gadd45a deletion, the exencephaly frequencies are increased (30.5% in the Gadd45a/Cdkn1a‐null embryos) and are similar to those in the Gadd45a/Trp53‐null embryos. Although XPC deletion increased exencephaly frequencies in Trp53‐null embryos, XPC deletion did not increase the exencephaly frequencies in Gadd45a‐null embryos.

CONCLUSIONS

The increased genetic liability to exencephaly in the Gadd45a/Trp53‐ and Gadd45a/Cdkn1a‐null embryos may be related to the disruption of multiple cellular pathways associated with Gadd45a and p53. Birth Defects Research (Part A), 2006. © 2006 Wiley‐Liss, Inc.