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.
A polymorphism (Rs1042522) in TP53 gene is a risk factor for down syndrome in sicilian mothers
Romano C.
2017-01-01
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
