Construction of a high-density genetic map for grape using specific length amplified fragment (SLAF) sequencing

20Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.

Abstract

Genetic maps are important tools in plant genomics and breeding. We report a large-scale discovery of single nucleotide polymorphisms (SNPs) using the specific length amplified fragment sequencing (SLAF-seq) technique for the construction of high-density genetic maps for two elite wine grape cultivars, ‘Chardonnay’ and ‘Beibinghong’, and their 130 F1 plants. A total of 372.53 M paired-end reads were obtained after preprocessing. The average sequencing depth was 33.81 for ‘Chardonnay’ (the female parent), 48.20 for ‘Beibinghong’ (the male parent), and 12.66 for the F1 offspring. We detected 202,349 high-quality SLAFs of which 144,972 were polymorphic; 10,042 SNPs were used to construct a genetic map that spanned 1,969.95 cM, with an average genetic distance of 0.23 cM between adjacent markers. This genetic map contains the largest molecular marker number of the grape maps so far reported. We thus demonstrate that SLAF-seq is a promising strategy for the construction of high-density genetic maps; the map that we report here is a good potential resource for QTL mapping of genes linked to major economic and agronomic traits, map-based cloning, and marker-assisted selection of grape.

Figures

  • Table 1. Summary of SLAF-seq data for grape.
  • Fig 1. Number of SLAFs (A) and average sequencing depths (B) of F1 population. The x-axis indicates the number of SLAFs (A) and the average depths (B); the y-axis indicates individual F1 offspring.
  • Table 2. Distribution of SLAFs and SNPs on chromosomes.
  • Fig 2. Genetic map lengths and marker distribution in 19 linkage groups of the female parent. Genetic distance is indicated by the vertical scale in centimorgans (cM). Black lines represent mapped markers. 1–19 represent corresponding linkage groups ID.
  • Table 3. The genetic length and markers number of 19 linkage groups.
  • Table 4. The markers spacing and coverage of 19 linkage groups.
  • Fig 3. Genetic map lengths and marker distribution in 19 linkage groups of the male parent.
  • Fig 4. Genetic lengths and marker distribution in 19 linkage groups of the integrated map.

References Powered by Scopus

The Sequence Alignment/Map format and SAMtools

41477Citations
N/AReaders
Get full text

Fast and accurate short read alignment with Burrows-Wheeler transform

35143Citations
N/AReaders
Get full text

A framework for variation discovery and genotyping using next-generation DNA sequencing data

8350Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Facing climate change: Biotechnology of iconic mediterranean woody crops

70Citations
N/AReaders
Get full text

Construction of a highly saturated Genetic Map for Vitis by Next-generation Restriction Site-associated DNA Sequencing

33Citations
N/AReaders
Get full text

A novel high-density grapevine (Vitis vinifera L.) integrated linkage map using GBS in a half-diallel population

30Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Wang, J., Su, K., Guo, Y., Xing, H., Zhao, Y., Liu, Z., … Guo, X. (2017). Construction of a high-density genetic map for grape using specific length amplified fragment (SLAF) sequencing. PLoS ONE, 12(7). https://doi.org/10.1371/journal.pone.0181728

Readers over time

‘17‘18‘19‘20‘21‘23‘24‘2502468

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 11

73%

Researcher 4

27%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 15

88%

Medicine and Dentistry 1

6%

Social Sciences 1

6%

Save time finding and organizing research with Mendeley

Sign up for free
0