The distribution and impact of common copy-number variation in the genome of the domesticated apple, Malus x domestica Borkh. (December 2015)
- Record Type:
- Journal Article
- Title:
- The distribution and impact of common copy-number variation in the genome of the domesticated apple, Malus x domestica Borkh. (December 2015)
- Main Title:
- The distribution and impact of common copy-number variation in the genome of the domesticated apple, Malus x domestica Borkh
- Authors:
- Boocock, James
Chagné, David
Merriman, Tony
Black, Michael - Abstract:
- Abstract Background Copy number variation (CNV) is a common feature of eukaryotic genomes, and a growing body of evidence suggests that genes affected by CNV are enriched in processes that are associated with environmental responses. Here we use next generation sequence (NGS) data to detect copy-number variable regions (CNVRs) within theMalus xdomestica genome, as well as to examine their distribution and impact. Methods CNVRs were detected using NGS data derived from 30 accessions ofM . xdomestica analyzed using the read-depth method, as implemented in the CNVrd2 software. To improve the reliability of our results, we developed a quality control and analysis procedure that involved checking for organelle DNA, not repeat masking, and the determination of CNVR identity using a permutation testing procedure. Results Overall, we identified 876 CNVRs, which spanned 3.5 % of the apple genome. To verify that detected CNVRs were not artifacts, we analyzed the B- allele-frequencies (BAF) within a single nucleotide polymorphism (SNP) array dataset derived from a screening of 185 individual apple accessions and found the CNVRs were enriched for SNPs having aberrant BAFs (P < 1e-13, Fisher's Exact test). Putative CNVRs overlapped 845 gene models and were enriched for resistance (R) gene models (P < 1e-22, Fisher's exact test). Of note was a cluster of resistance gene models on chromosome 2 near a region containing multiple major gene loci conferring resistance to apple scab.Abstract Background Copy number variation (CNV) is a common feature of eukaryotic genomes, and a growing body of evidence suggests that genes affected by CNV are enriched in processes that are associated with environmental responses. Here we use next generation sequence (NGS) data to detect copy-number variable regions (CNVRs) within theMalus xdomestica genome, as well as to examine their distribution and impact. Methods CNVRs were detected using NGS data derived from 30 accessions ofM . xdomestica analyzed using the read-depth method, as implemented in the CNVrd2 software. To improve the reliability of our results, we developed a quality control and analysis procedure that involved checking for organelle DNA, not repeat masking, and the determination of CNVR identity using a permutation testing procedure. Results Overall, we identified 876 CNVRs, which spanned 3.5 % of the apple genome. To verify that detected CNVRs were not artifacts, we analyzed the B- allele-frequencies (BAF) within a single nucleotide polymorphism (SNP) array dataset derived from a screening of 185 individual apple accessions and found the CNVRs were enriched for SNPs having aberrant BAFs (P < 1e-13, Fisher's Exact test). Putative CNVRs overlapped 845 gene models and were enriched for resistance (R) gene models (P < 1e-22, Fisher's exact test). Of note was a cluster of resistance gene models on chromosome 2 near a region containing multiple major gene loci conferring resistance to apple scab. Conclusion We present the first analysis and catalogue of CNVRs in theM . xdomestic a genome. The enrichment of the CNVRs with R gene models and their overlap with gene loci of agricultural significance draw attention to a form of unexplored genetic variation in apple. This research will underpin further investigation of the role that CNV plays within the apple genome. … (more)
- Is Part Of:
- BMC genomics. Volume 16:Number 1(2015)
- Journal:
- BMC genomics
- Issue:
- Volume 16:Number 1(2015)
- Issue Display:
- Volume 16, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 1
- Issue Sort Value:
- 2015-0016-0001-0000
- Page Start:
- 1
- Page End:
- 15
- Publication Date:
- 2015-12
- Subjects:
- Genomes -- Periodicals
Gene mapping -- Periodicals
Genomics -- Periodicals
Base Sequence -- Periodicals
Chromosome Mapping -- Periodicals
Genetic Techniques -- Periodicals
Sequence Analysis, DNA -- Periodicals
572.8605 - Journal URLs:
- http://www.biomedcentral.com/bmcgenomics/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=32 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12864-015-2096-x ↗
- Languages:
- English
- ISSNs:
- 1471-2164
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9848.xml