A high-density genetic map and molecular sex-typing assay for gerbils
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In: Mammalian Genome, Vol. 30, No. 3-4, 04.2019, p. 63-70.
Research output: Contribution to journal › Article › peer-review
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T1 - A high-density genetic map and molecular sex-typing assay for gerbils
AU - Brekke, Thomas
AU - Mulley, John
AU - Steele, Katherine
AU - Denver, Megan
AU - Thom, Angharad
AU - Supriya, Sushmita
PY - 2019/4
Y1 - 2019/4
N2 - We constructed a high-density genetic map for Mongolian gerbils (Meriones unguiculatus). We genotyped 137 F2 individuals with a genotype-by-sequencing (GBS) approach at over 10,000 loci and built the genetic map using a two-step approach. First, we chose the highest-quality set of 485 markers to construct a robust map of 1239 cM with 22 linkage groups as expected from the published karyotype. Second, we added an additional 5449 markers onto the map based on their genotype similarity with the original markers. We used the final marker set to assemble 1140 genomic scaffolds (containing ~ 20% of annotated genes) into a chromosome-level assembly. We used both genetic linkage and relative sequencing coverage in males and females to identify X- and Y-chromosome scaffolds and from these we designed a robust and internally-controlled PCR assay to determine sex. This assay will facilitate early stage sex-typing of embryonic and young gerbils which is difficult using current visual methods
AB - We constructed a high-density genetic map for Mongolian gerbils (Meriones unguiculatus). We genotyped 137 F2 individuals with a genotype-by-sequencing (GBS) approach at over 10,000 loci and built the genetic map using a two-step approach. First, we chose the highest-quality set of 485 markers to construct a robust map of 1239 cM with 22 linkage groups as expected from the published karyotype. Second, we added an additional 5449 markers onto the map based on their genotype similarity with the original markers. We used the final marker set to assemble 1140 genomic scaffolds (containing ~ 20% of annotated genes) into a chromosome-level assembly. We used both genetic linkage and relative sequencing coverage in males and females to identify X- and Y-chromosome scaffolds and from these we designed a robust and internally-controlled PCR assay to determine sex. This assay will facilitate early stage sex-typing of embryonic and young gerbils which is difficult using current visual methods
KW - Animals
KW - Chromosome Mapping
KW - Female
KW - Genetic Linkage
KW - Genetic Markers
KW - Genome
KW - Genomics
KW - Gerbillinae/genetics
KW - Male
KW - Molecular Typing
KW - Polymorphism, Single Nucleotide
KW - Sex Chromosomes/genetics
U2 - 10.1007/s00335-019-09799-z
DO - 10.1007/s00335-019-09799-z
M3 - Article
C2 - 30972478
VL - 30
SP - 63
EP - 70
JO - Mammalian Genome
JF - Mammalian Genome
SN - 0938-8990
IS - 3-4
ER -