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A high-density genetic map for P genome of Agropyron Gaertn. based on specific-locus amplified fragment sequencing (SLAF-seq)

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Abstract

Main conclusion

This genetic map for Agropyron Gaertn. contained 1023 markers on seven linkage groups, with a total of 907.8 cM and an average distance of 1.5 cM between adjacent loci.

Many wheat- Agropyron cristatum derivative lines exhibit superior agronomic traits, and part of them are valuable for future wheat breeding. To date, no high-density genetic map for Agropyron Gaertn. has been published. Specific-locus amplified fragment sequencing (SLAF-seq), a recently developed strategy for large scale de novo discovery and genotyping of single nucleotide polymorphisms (SNPs), was employed in this study to develop sufficient markers for a segregating Agropyron F1 population derived from an interspecific cross between two cross-pollinated diploid collections A. cristatum (L.) Beauv. ‘Z1842’ and A. mongolicum Keng ‘Z2098’. In total, we obtained raw data consisting of 128,932,358 pair-end reads of ~80 bp long after sequencing. Then 69,325 high-quality SLAFs were detected, of which 26,248 SLAFs were polymorphic and 1752 of the polymorphic markers were used for the genetic map construction. The final map contained 1023 markers on the seven linkage groups (LGs), which spanned a total of 907.8 cM with an average number of 146 markers and 89 loci per LG and an average distance of 1.5 cM between adjacent loci. To our knowledge, this map is the densest genetic linkage map for Agropyron so far. Through BLAT alignment of Agropyron SLAF marker sequences with the draft genome assemblies of wheat and barley, the Agropyron LGs were assigned as LG1-7 according to their corresponding homoeologous chromosomal groups of wheat. Results of this study will not only provide a platform for gene/QTL fine mapping, but also serve as a reference to assist the assembling of the P genome sequence in future.

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Abbreviations

Agropyron :

Agropyron Gaertn.

CP:

Cross-pollinated

LG:

Linkage group

SLAF-seq:

Specific-locus amplified fragment sequencing

SNP:

Single nucleotide polymorphism

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Acknowledgments

This work was supported by the grants from the National Basic Research Program of China (973 Grant No. 2011CB100104), the National Natural Science Foundation of China (Grant No. 31471493), and the National High Technology Research and Development Program of China (863 Grant No. 2011AA100101).

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Corresponding author

Correspondence to Lihui Li.

Additional information

Y. Zhang, J. Zhang and L. Huang contributed equally to this work.

Electronic supplementary material

Below is the link to the electronic supplementary material.

425_2015_2372_MOESM1_ESM.tif

Supplementary material 1 (TIFF 952 kb). Fig. S1 Examples for the five segregation types for population type CP. * indicates SNP. P, paternal parent; M, maternal parent. aa, ab and ac are tags for three individuals. The number under P, M, aa, ab and ac indicates sequencing depth. “XXXXXXXXXX” represents middle unknown fragment in a marker sequence, and the base number is also unknown. According to JoinMap 4 manual, < ab × ad > , locus heterozygous in both parents, four alleles; < ef × eg > , locus heterozygous in both parents, three alleles; < hk × hk > , locus heterozygous in both parents, two alleles; < lm × ll > , locus heterozygous in the first parents, two alleles; < nn × np > , locus heterozygous in the second parents, two alleles

Supplementary material 2 (PNG 2346 kb). Fig. S2 Linkage group 1 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 3 (PNG 3541 kb). Fig. S3 Linkage group 2 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 4 (PNG 1400 kb). Fig. S4 Linkage group 3 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 5 (PNG 1438 kb). Fig. S5 Linkage group 4 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 6 (PNG 2754 kb). Fig. S6 Linkage group 5 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 7 (PNG 1224 kb). Fig. S7 Linkage group 6 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 8 (PNG 2438 kb). Fig. S8 Linkage group 7 for Z2098 (female), Z1842 (male) and their integration

Supplementary material 9 (TIFF 1649 kb). Fig. S9 Spike phenotype of the parents and individuals of F1 population

Supplementary material 10 (PDF 31 kb)

425_2015_2372_MOESM11_ESM.xlsx

Supplementary material 11 (XLSX 786 kb). Table S4 Genotype data of 1752 SLAF markers in the F1 individuals for the map construction

Supplementary material 12 (XLSX 63 kb). Table S5 Positions of SLAF markers on the seven linkage groups

425_2015_2372_MOESM13_ESM.xlsx

Supplementary material 13 (XLSX 39 kb). Table S6 Genotype frequencies of segregation distortion SLAF markers in the F1 individuals

425_2015_2372_MOESM14_ESM.xlsx

Supplementary material 14 (XLSX 81 kb). Table S7 Partial sequences of contigs of wheat and barley showing ≥ 80 % sequence identity with Agropyron marker sequences

425_2015_2372_MOESM15_ESM.xlsx

Supplementary material 15 (XLSX 24 kb). Table S8 Genetic positions of Agropyron markers and their homologous contigs in wheat and barley. The contigs, which were homologous with Agropyron markers and had no information about chromosomal localization and genetic position, were also listed

Supplementary material 16 (XLSX 160 kb). Table S9 Sequences of 1752 SLAF markers used for the map construction

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Zhang, Y., Zhang, J., Huang, L. et al. A high-density genetic map for P genome of Agropyron Gaertn. based on specific-locus amplified fragment sequencing (SLAF-seq). Planta 242, 1335–1347 (2015). https://doi.org/10.1007/s00425-015-2372-7

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  • DOI: https://doi.org/10.1007/s00425-015-2372-7

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