A polymorphism (rs1042522) in TP53 gene is a risk factor for Down Syndrome in Sicilian mothers

Abstract

Objective: Trisomy 21 is the most frequent genetic cause of intellectual disability. Tumor Protein 53 (TP53) gene down-regulation triggers chromosomal instability. A TP53 gene polymorphism c.215G > C (rs1042522) is associated with accumulation of aneuploid cells. We analyzed the TP53 c.215G > C (rs1042522) polymorphism in Sicilian mothers of subjects with Down Syndrome (DS) within a case-control study.

Methods: Nucleotide polymorphism was detected by pyrosequencing technology.

Results: The distribution of TP53 c.215G > C polymorphism showed significant difference between mothers of subjects with DS and controls.

Conclusions: Our data show that TP53 c.215G > C polymorphism is a risk factor for DS in Sicilian mothers.

Keywords:

• Mothers of Down Syndrome
• Down Syndrome
• Trisomy 21
• TP53 c.215G > C polymorphism
• pyrosequencing

Disclosure statement

The authors report no conflicts of interest.