A dense genetic linkage map for common carp and its integration with a BAC-based physical map

PLoS One. 2013 May 21;8(5):e63928. doi: 10.1371/journal.pone.0063928. Print 2013.

Abstract

Background: Common carp (Cyprinus carpio) is one of the most important aquaculture species with an annual global production of 3.4 million metric tons. It is also an important ornamental species as well as an important model species for aquaculture research. To improve the economically important traits of this fish, a number of genomic resources and genetic tools have been developed, including several genetic maps and a bacterial artificial chromosome (BAC)-based physical map. However, integrated genetic and physical maps are not available to study quantitative trait loci (QTL) and assist with fine mapping, positional cloning and whole genome sequencing and assembly. The objective of this study was to integrate the currently available BAC-based physical and genetic maps.

Results: The genetic map was updated with 592 novel markers, including 312 BAC-anchored microsatellites and 130 SNP markers, and contained 1,209 genetic markers on 50 linkage groups, spanning 3,565.9 cM in the common carp genome. An integrated genetic and physical map of the common carp genome was then constructed, which was composed of 463 physical map contigs and 88 single BACs. Combined lengths of the contigs and single BACs covered a physical length of 498.75 Mb, or around 30% of the common carp genome. Comparative analysis between common carp and zebrafish genomes was performed based on the integrated map, providing more insights into the common carp specific whole genome duplication and segmental rearrangements in the genome.

Conclusion: We integrated a BAC-based physical map to a genetic linkage map of common carp by anchoring BAC-associated genetic markers. The density of the genetic linkage map was significantly increased. The integrated map provides a tool for both genetic and genomic studies of common carp, which will help us to understand the genomic architecture of common carp and facilitate fine mapping and positional cloning of economically important traits for genetic improvement and modification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carps / genetics*
  • Chromosomes / genetics
  • Chromosomes, Artificial, Bacterial / genetics*
  • Conserved Sequence / genetics
  • Genetic Linkage*
  • Genetic Loci / genetics
  • Genetic Markers
  • Genome / genetics
  • Microsatellite Repeats / genetics
  • Physical Chromosome Mapping*
  • Polymorphism, Single Nucleotide / genetics
  • Synteny / genetics
  • Zebrafish / genetics

Substances

  • Genetic Markers

Grants and funding

This study was supported by the grants from National Department Public Benefit Research Foundation (No. 200903045), National High-tech Research & Development Program of China (No. 2009AA10Z105 and 2011AA100401), China Ministry of Agriculture “948” Program (No. 2010-Z11 and 2011-G12) and Research Foundation of Chinese Academy of Fishery Sciences (No. 2009B002). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.