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.2020 Feb 18;9(2):270.
doi: 10.3390/plants9020270.

Rooibos (Aspalathus linearis) Genome Size Estimation Using Flow Cytometry and K-Mer Analyses

Affiliations

Rooibos (Aspalathus linearis) Genome Size Estimation Using Flow Cytometry and K-Mer Analyses

Yamkela Mgwatyu et al. Plants (Basel)..

Abstract

Plant genomes provide information on biosynthetic pathways involved in the production of industrially relevant compounds. Genome size estimates are essential for the initiation of genome projects. The genome size of rooibos (Aspalathus linearis species complex) was estimated using DAPI flow cytometry and k-mer analyses. For flow cytometry, a suitable nuclei isolation buffer, plant tissue and a transport medium for rooibos ecotype samples collected from distant locations were identified. When using radicles from commercial rooibos seedlings, Woody Plant Buffer andVicia faba as an internal standard, the flow cytometry-estimated genome size of rooibos was 1.24 ± 0.01 Gbp. The estimates for eight wild rooibos growth types did not deviate significantly from this value. K-mer analysis was performed using Illumina paired-end sequencing data from one commercial rooibos genotype. For biocomputational estimation of the genome size, four k-mer analysis methods were investigated: A standard formula and three popular programs (BBNorm, GenomeScope, and FindGSE). GenomeScope estimates were strongly affected by parameter settings, specifically CovMax. When using the complete k-mer frequency histogram (up to 9 × 105), the programs did not deviate significantly, estimating an average rooibos genome size of 1.03 ± 0.04 Gbp. Differences between the flow cytometry and biocomputational estimates are discussed.

Keywords: Aspalathus linearis; ITS region; Rooibos; flow cytometry; genome size; k-mer analysis.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flow cytometry histograms forA. linearis leaves from 3 weeks-old commercial rooibos seedlings using Partec buffer (A), LBO1 10X Triton X-100 buffer (B), LBO1 5X Triton X-100 (C), and Woody Plant Buffer (D). Sample 2C (GO/G1 phase) peaks are shown (n = 10).
Figure 2
Figure 2
Flow cytometry histograms of rooibos radicles (A) and cotyledons (B), as well as fresh leaves (C) and silica-dried leaves (D) from two-months-old commercial rooibos seedlings. 2C (G0/G1 phase), 4C (G2 phase) and reference standard (Vicia faba; 2C=26.66 pg) 2C peaks are shown. (n = 10).
Figure 3
Figure 3
Flow cytometry genome size estimates for different rooibos growth types using silica-dried leaf samples (RC = Red Commercial (n = 10), RE = Red Escaped (n = 5), RW = Red Wild (n = 6), WT = Wupperthal Type (n = 9), TT = Tree Type (n = 5), GS = Grey Sprouter (n = 5), NiS=Nieuwoudtville Sprouter (n = 11), NS = Northern Sprouter (n = 5), AT = Algeria Type (n = 5), NT = Nardouwsberg Type (n = 4)).
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