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Free Content Changes in genome content generated via segregation of non‐allelic homologs

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Summary

A careful analysis of two maize recombinant inbred lines (RILs) relative to their inbred parents revealed the presence of several hundred apparently de novo copy number variants (CNVs). These changes in genome content were validated via both PCR and whole exome‐array capture‐and‐sequencing experiments. One hundred and eighty‐five genomic regions, which overlap with 38 high‐confidence genes, exhibited apparently de novo copy number variation (CNV) in these two RILs and in many instances the same apparently de novo CNV events were observed in multiple RILs. Further analyses revealed that these recurrent apparently de novo CNVs were caused by segregation of single‐copy homologous sequences that are located in non‐allelic positions in the two parental inbred lines. F1 individuals derived from these inbred lines will be hemizygous for each of these non‐allelic homologs but RIL genotypes will contain these sequences at zero, one or two genomic loci. Hence, the segregation of non‐allelic homologs may contribute to transgressive segregation. Indeed, statistical associations between phenotypic quantitative trait loci and genomic losses were observed for two of 14 tested pairs of non‐allelic homologs.
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Document Type: Research Article

Affiliations: 1: Department of Agronomy, 2035 Roy J. Carver Co-Lab, Iowa State University, Ames, IA 50011, USA 2: Interdepartmental Genetics, 2035 Roy J. Carver Co-Lab, Iowa State University, Ames, IA 50011, USA 3: Research Informatics, Roche NimbleGen, 500 South Rosa Road, Madison, WI 53705, USA 4: Development and Research, Roche NimbleGen, 500 South Rosa Road, Madison, WI 53705, USA 5: State Key Lab of Agrobiotechnology, China Agriculture University, Beijing, China 6: Department of Plant Biology, 250 Biological Science Center, St Paul, MN 55108, USA 7: Department of Statistics, 2115 Snedecor, Iowa State University, Ames, IA 50011, USA

Publication date: November 1, 2012

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