Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes

Population genetic studies of nonmodel organisms frequently employ reduced representation library (RRL) methodologies, many of which rely on protocols in which genomic DNA is digested by one or more restriction enzymes. However, because high molecular weight DNA is recommended for these protocols, s...

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Main Authors: Barreiro, F., Vieira, F., Martin, M., Haile, J., Gilbert, Thomas, Wales, N.
Format: Journal Article
Published: Wiley-Blackwell 2017
Online Access:http://hdl.handle.net/20.500.11937/52037
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author Barreiro, F.
Vieira, F.
Martin, M.
Haile, J.
Gilbert, Thomas
Wales, N.
author_facet Barreiro, F.
Vieira, F.
Martin, M.
Haile, J.
Gilbert, Thomas
Wales, N.
author_sort Barreiro, F.
building Curtin Institutional Repository
collection Online Access
description Population genetic studies of nonmodel organisms frequently employ reduced representation library (RRL) methodologies, many of which rely on protocols in which genomic DNA is digested by one or more restriction enzymes. However, because high molecular weight DNA is recommended for these protocols, samples with degraded DNA are generally unsuitable for RRL methods. Given that ancient and historic specimens can provide key temporal perspectives to evolutionary questions, we explored how custom-designed RNA probes could enrich for RRL loci (Restriction Enzyme-Associated Loci baits, or REALbaits). Starting with genotyping-by-sequencing (GBS) data generated on modern common ragweed (Ambrosia artemisiifolia L.) specimens, we designed 20 000 RNA probes to target well-characterized genomic loci in herbarium voucher specimens dating from 1835 to 1913. Compared to shotgun sequencing, we observed enrichment of the targeted loci at 19- to 151-fold. Using our GBS capture pipeline on a data set of 38 herbarium samples, we discovered 22 813 SNPs, providing sufficient genomic resolution to distinguish geographic populations. For these samples, we found that dilution of REALbaits to 10% of their original concentration still yielded sufficient data for downstream analyses and that a sequencing depth of ~7M reads was sufficient to characterize most loci without wasting sequencing capacity. In addition, we observed that targeted loci had highly variable rates of success, which we primarily attribute to similarity between loci, a trait that ultimately interferes with unambiguous read mapping. Our findings can help researchers design capture experiments for RRL loci, thereby providing an efficient means to integrate samples with degraded DNA into existing RRL data sets.
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spelling curtin-20.500.11937-520372017-10-06T06:13:59Z Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes Barreiro, F. Vieira, F. Martin, M. Haile, J. Gilbert, Thomas Wales, N. Population genetic studies of nonmodel organisms frequently employ reduced representation library (RRL) methodologies, many of which rely on protocols in which genomic DNA is digested by one or more restriction enzymes. However, because high molecular weight DNA is recommended for these protocols, samples with degraded DNA are generally unsuitable for RRL methods. Given that ancient and historic specimens can provide key temporal perspectives to evolutionary questions, we explored how custom-designed RNA probes could enrich for RRL loci (Restriction Enzyme-Associated Loci baits, or REALbaits). Starting with genotyping-by-sequencing (GBS) data generated on modern common ragweed (Ambrosia artemisiifolia L.) specimens, we designed 20 000 RNA probes to target well-characterized genomic loci in herbarium voucher specimens dating from 1835 to 1913. Compared to shotgun sequencing, we observed enrichment of the targeted loci at 19- to 151-fold. Using our GBS capture pipeline on a data set of 38 herbarium samples, we discovered 22 813 SNPs, providing sufficient genomic resolution to distinguish geographic populations. For these samples, we found that dilution of REALbaits to 10% of their original concentration still yielded sufficient data for downstream analyses and that a sequencing depth of ~7M reads was sufficient to characterize most loci without wasting sequencing capacity. In addition, we observed that targeted loci had highly variable rates of success, which we primarily attribute to similarity between loci, a trait that ultimately interferes with unambiguous read mapping. Our findings can help researchers design capture experiments for RRL loci, thereby providing an efficient means to integrate samples with degraded DNA into existing RRL data sets. 2017 Journal Article http://hdl.handle.net/20.500.11937/52037 10.1111/1755-0998.12610 Wiley-Blackwell restricted
spellingShingle Barreiro, F.
Vieira, F.
Martin, M.
Haile, J.
Gilbert, Thomas
Wales, N.
Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
title Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
title_full Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
title_fullStr Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
title_full_unstemmed Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
title_short Characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
title_sort characterizing restriction enzyme-associated loci in historic ragweed (ambrosia artemisiifolia) voucher specimens using custom-designed rna probes
url http://hdl.handle.net/20.500.11937/52037