Rapid single nucleotide polymorphism mapping in <it>C. elegans</it>
<p>Abstract</p> <p>Background</p> <p>In <it>C. elegans</it>, single nucleotide polymorphisms (SNPs) can function as silent genetic markers, with applications ranging from classical two- and three-factor mapping to measuring recombination across whole chromos...
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Online Access: | http://www.biomedcentral.com/1471-2164/6/118 |
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doaj-c4f333a27b34454ea11e5a522d64a87a2020-11-25T00:04:12ZengBMCBMC Genomics1471-21642005-09-016111810.1186/1471-2164-6-118Rapid single nucleotide polymorphism mapping in <it>C. elegans</it>Hullett PatrickHarrach TraceyHammarlund MarcDavis M WayneOlsen ShawnJorgensen Erik M<p>Abstract</p> <p>Background</p> <p>In <it>C. elegans</it>, single nucleotide polymorphisms (SNPs) can function as silent genetic markers, with applications ranging from classical two- and three-factor mapping to measuring recombination across whole chromosomes.</p> <p>Results</p> <p>Here, we describe a set of 48 primer pairs that flank SNPs evenly spaced across the <it>C. elegans </it>genome and that work under identical PCR conditions. Each SNP in this set alters a <it>Dra</it>I site, enabling rapid and parallel scoring. We describe a procedure using these reagents to quickly and reliably map mutations. We show that these techniques correctly map a known gene, <it>dpy-5</it>. We then use these techniques to map mutations in an uncharacterized strain, and show that its behavioral phenotype can be simultaneously mapped to three loci.</p> <p>Conclusion</p> <p>Together, the reagents and methods described represent a significant advance in the accurate, rapid and inexpensive mapping of genes in <it>C. elegans</it>.</p> http://www.biomedcentral.com/1471-2164/6/118 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hullett Patrick Harrach Tracey Hammarlund Marc Davis M Wayne Olsen Shawn Jorgensen Erik M |
spellingShingle |
Hullett Patrick Harrach Tracey Hammarlund Marc Davis M Wayne Olsen Shawn Jorgensen Erik M Rapid single nucleotide polymorphism mapping in <it>C. elegans</it> BMC Genomics |
author_facet |
Hullett Patrick Harrach Tracey Hammarlund Marc Davis M Wayne Olsen Shawn Jorgensen Erik M |
author_sort |
Hullett Patrick |
title |
Rapid single nucleotide polymorphism mapping in <it>C. elegans</it> |
title_short |
Rapid single nucleotide polymorphism mapping in <it>C. elegans</it> |
title_full |
Rapid single nucleotide polymorphism mapping in <it>C. elegans</it> |
title_fullStr |
Rapid single nucleotide polymorphism mapping in <it>C. elegans</it> |
title_full_unstemmed |
Rapid single nucleotide polymorphism mapping in <it>C. elegans</it> |
title_sort |
rapid single nucleotide polymorphism mapping in <it>c. elegans</it> |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2005-09-01 |
description |
<p>Abstract</p> <p>Background</p> <p>In <it>C. elegans</it>, single nucleotide polymorphisms (SNPs) can function as silent genetic markers, with applications ranging from classical two- and three-factor mapping to measuring recombination across whole chromosomes.</p> <p>Results</p> <p>Here, we describe a set of 48 primer pairs that flank SNPs evenly spaced across the <it>C. elegans </it>genome and that work under identical PCR conditions. Each SNP in this set alters a <it>Dra</it>I site, enabling rapid and parallel scoring. We describe a procedure using these reagents to quickly and reliably map mutations. We show that these techniques correctly map a known gene, <it>dpy-5</it>. We then use these techniques to map mutations in an uncharacterized strain, and show that its behavioral phenotype can be simultaneously mapped to three loci.</p> <p>Conclusion</p> <p>Together, the reagents and methods described represent a significant advance in the accurate, rapid and inexpensive mapping of genes in <it>C. elegans</it>.</p> |
url |
http://www.biomedcentral.com/1471-2164/6/118 |
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