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A new software tool detects chromosomal alterations present in only a subset of cells in the body. This method, described 31 May in BMC Genomics, may help reveal mosaicism’s contribution to neurological disorders1.
Among the most well-known examples of mosaicism is X-chromosome inactivation in women: One of the two X chromosomes in each woman is randomly turned off in different sets of cells, so that some cells express genes from one chromosome and some from the other. Spontaneous mutations during cell division may also cause some cells to have genes that are different from those in the rest of the body.
The new technique may allow researchers to identify instances of mosaicism in large databases of genomic information.
The researchers designed an algorithm called triPOD, for parent-of-origin-based detection in trios — the affected individual and his or her two parents. TriPOD looks at variations, or polymorphisms, in a single nucleotide. It compares these single nucleotide polymorphisms (SNPs) in the parents and then predicts the expected variants in their child.
For example, if both copies in the mother are variant A and both copies in the father are variant B, the child would be expected to have one copy of A and one copy of B. If some cells in the child have a different combination of variants, it suggests the presence of mosaicism.
The software program analyzes 600,000 SNPs for each trio of individuals. It then annotates the identified abnormalities on a reference genome.
Using this method, the researchers looked at mosaicism in 1,587 trios from the Autism Genetic Resource Exchange, a database of families that have more than one child with autism. They found 49 such events in this group. However, some of the mosaicism may have occurred when researchers cultured cells from the individuals, and may not be present in their bodies, the researchers note.
1: Baugher J.D. et al. BMC Genomics 14, 367 (2013) PubMed