ScienceDaily (Oct. 3, 2011) Chromosomal abnormalities linked to intellectual disability can be traced back to the father, particularly those who are older when the child is conceived, finds research published online in the Journal of Medical Genetics.
Chromosomal abnormalities are caused by copy number variations, or CNVs. These are structural variations resulting in missing, repeated, inverted or misplaced DNA sequences in cells.
They can be inherited or arise anew, and are a common cause of disease. However, little is known about how CNVs are formed, for example, if they occur more frequently on the DNA sequence passed on by the mother or the father, or if parental age is important.
The research team systematically analysed the prevalence of rare CNVs in almost 3500 people with intellectual disabilities between 2006 and 2010.
They found CNVs which had arisen anew, as opposed to being inherited, in 227 people, meaning the prevalence was around twice as common in this group as among people with autism and three times as common as among those with asthma.
Further analysis to determine the parental origin of the CNVs in the 118 people for whom data were available, showed that 90 had come from the father, and that three quarters represented missing DNA sequences.
The researchers compared the father’s age at time of birth in the group with CNVs with people with no intellectual disability, matching for ethnicity and era of birth to minimise the impact of any cultural or social factors. But they found no differences in paternal age between the two groups.
The researchers then divided people with CNVs into two groups — those with CNVs occurring in regions of the genome with highly repetitive DNA sequences, and those with CNVs occurring in non — repetitive DNA sequences.
They also compared paternal ages in both groups with those of the people without any intellectual disability.
A significant increase in the father’s age was found in the group of CNVs in non- repetitive DNA sequences — which accounted for most CNVs — providing a crucial insight into the understanding of how and why disease — causing CNVs are formed, say the authors.
The findings also indicate that newly arising CNVs not only originate more often from the father’s DNA, but that the father’s age has a role, the authors add.
“In conclusion, our data provide for the first time convincing evidence that CNVs in intellectual disability are largely paternal in origin,” they write.
And they suggest that both the gender and age bias can be explained by ongoing cell divisions of self — renewing sperm cells during the fetal development of boys — with the potential for mistakes — as well as impaired DNA genesis and repair as a consequence of the aging process.
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The above story is reprinted (with editorial adaptations by ScienceDaily staff) from materials provided by BMJ-British Medical Journal, via EurekAlert!, a service of AAAS.
- Jayne Y. Hehir-Kwa, Benjamín Rodríguez-Santiago, Lisenka E. Vissers, Nicole de Leeuw, Rolph Pfundt, Jan K. Buitelaar, Luis A. Pérez-Jurado, Joris A. Veltman. De novo copy number variants associated with intellectual disability have a paternal origin and age bias. Journal of Medical Genetics, 2011; DOI: 10.1136/jmedgenet-2011-100147
Note: If no author is given, the source is cited instead.
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