Adamek Kristian, Jones Andrew Maxwell Phineas, Torkamaneh Davoud
Dep. of Plant Agriculture, Univ. of Guelph, Guelph, ON, N1G 2W1, Canada.
Dép. de Phytologie, Univ. Laval, Québec, QC, G1V 0A6, Canada.
Plant Genome. 2022 Mar;15(1):e20169. doi: 10.1002/tpg2.20169. Epub 2021 Nov 22.
Cannabis (Cannabis sativa L.) is typically propagated using stem cuttings taken from mother plants to produce genetically uniform propagules. However, producers anecdotally report that clonal lines deteriorate over time and eventually produce clones with less vigor and lower cannabinoid levels than the original mother plant. While the cause of this deterioration has not been investigated, one potential contributor is the accumulation of somatic mutations within the plant. To test this, we used deep sequencing of whole genomes (>50×) to compare the variability within an individual cannabis cultivar Honey Banana plant sampled at the bottom, middle, and top. We called over six million sequence variants based on a reference genome and found that the top had the most by a sizable amount. Comparing the variants among the samples uncovered that nearly 600,000 (34%) were unique to the top while the bottom only contained 148,000 (12%), and middle with 77,000 (9%) unique variants. Bioinformatics tools were used to identify mutations in critical cannabinoid-terpene biosynthesis pathways. While none were identified as high impact, four genes contained more than double the average level of nucleotide diversity (π) in or near the gene. Two genes code for essential enzymes required for the cannabinoid pathway while the other two are in the terpene pathways, demonstrating that mutations were accumulating within these pathways and could influence their function. Overall, a measurable number of intraplant genetic diversity was discovered that could impact long-term genetic fidelity of clonal lines and potentially contribute to the observed decline in vigor and cannabinoid content.
大麻(Cannabis sativa L.)通常通过从母株上截取茎段进行繁殖,以产生基因一致的繁殖体。然而,种植者有传闻称,克隆品系会随着时间推移而退化,最终产生的克隆体活力不如原始母株,大麻素水平也更低。虽然这种退化的原因尚未得到研究,但一个潜在因素可能是植物体内体细胞突变的积累。为了验证这一点,我们对整个基因组进行了深度测序(>50×),以比较同一株大麻品种“蜂蜜香蕉”底部、中部和顶部样本的变异性。基于参考基因组,我们鉴定出超过600万个序列变异,发现顶部的变异数量最多。比较样本之间的变异发现,近60万个(34%)变异是顶部独有的,而底部仅包含14.8万个(12%),中部有7.7万个(9%)独特变异。我们使用生物信息学工具来识别关键大麻素 - 萜烯生物合成途径中的突变。虽然没有发现高影响的突变,但有四个基因在基因内部或附近的核苷酸多样性(π)平均水平的两倍以上。其中两个基因编码大麻素途径所需的关键酶,另外两个在萜烯途径中,这表明这些途径中正在积累突变,可能会影响其功能。总体而言,我们发现了植物内部可测量的遗传多样性,这可能会影响克隆品系的长期遗传稳定性,并可能导致观察到的活力和大麻素含量下降。