Telomere Length in Plants Estimated with Long Read Sequencing
Kelly Colt,
Semar Petrus,
Bradley W. Abramson
et al.
Abstract:Telomeres play an important role in chromosome stability and their length is thought to be related to an organism's lifestyle and lifespan. Telomere length is variable across plant species and between cultivars of the same species, possibly conferring adaptive advantage. However, it is not known whether telomere length is related to lifestyle or life span across a diverse array of plant species due to the lack of information on telomere length in plants. Here we leverage genomes assembled with long read sequen… Show more
“…In Arabidopsis thaliana , loss of the RPA1B ortholog is sensitive to Ultraviolet B (UV-B) light with reduced chlorophyll A and B and inhibited root growth, which is due to elevated DNA damage 33 . It is thought that long lived organisms actively protect their telomere length 35,36 , and repair their DNA 37,38 .…”
Section: Resultsmentioning
confidence: 99%
“…In addition, telomere sequences were assembled on the ends of most chromosomes, and these telomeres were long compared to other plants with maximum sequences spanning 30 kb as compared to the model plants Arabidopsis thaliana and Zea mays that have 3-5 kb telomeres (Fig. 3b; Supplementary Table 3) 35 . In the Ad77271a genome, we assembled a total of 300 Kb of the ribosomal DNA (rDNA) with only one 26S array that included 35 copies on Chr38, and one 5S array that included 442 copies on Ad77271a Chr01 (Supplementary Table 4).…”
Section: Resultsmentioning
confidence: 99%
“…s 3a; d; e). In general, the centromere arrays assembled well into 1-2 Mb regions that were both metacentric as well as acrocentric (Chr12, 24,26,28,35,38,39 are acrocentric; Supplementary Fig. 9).…”
Section: Baobab Genome Organization: Centromere Telomere Rdna and Dna...mentioning
confidence: 97%
“…In Arabidopsis thaliana, loss of the RPA1B ortholog is sensitive to Ultraviolet B (UV-B) light with reduced chlorophyll A and B and inhibited root growth, which is due to elevated DNA damage 33 . It is thought that long lived organisms actively protect their telomere length 35,36 , and repair their DNA 37,38 . Since the K-mer frequency analysis yielded a haploid genome size of approximately 750 Mb (Table 1) and a graph structure indicative of high heterozygosity ( Fig.…”
Section: Baobab Genome Assembly Annotation and Ploidy Estimationmentioning
Baobab,Adansonia digitata, is a long-lived tree endemic to Africa that holds great economic, ecological, and cultural value. However, our knowledge of its genomic features, evolutionary history, and diversity is limited, rendering it orphaned scientifically. We generated a haploid chromosome-level reference genome anchored into 42 chromosomes forA. digitata, as well as draft assemblies for a sibling tree, two trees from distinct locations in Africa, and a related species,A. zafrom Madagascar. Unlike any other plant to date, DNA transposable elements (TEs) make up 33% of theA. digitatagenome compared to only 10% long terminal repeat retrotransposons (LTR-RTs), which are usually predominant in plant genomes. Baobab has undergone a whole genome duplication (WGD) shared with the Malvoideae ∼30 million years ago (MYA), as well as a confirmed autotetraplody event 3-4 million MYA that coincides with the most recent burst of TE insertions. Resequencing 25A. digitatatrees from Africa revealed three subpopulations that suggest gene flow through most of West Africa but separated from East Africa. Gene enrichment analysis for baobab-specific and high fixation index (Fst) suggested baobab may have retained multiple copies of circadian, light and growth genes to coordinate genome protection for longevity through theUV RESISTANCE LOCUS 8(UVR8) and synchronizing flower development with pollinators. This study lays the groundwork for the creation of breeding resources and the conservation of baobab biodiversity.
“…In Arabidopsis thaliana , loss of the RPA1B ortholog is sensitive to Ultraviolet B (UV-B) light with reduced chlorophyll A and B and inhibited root growth, which is due to elevated DNA damage 33 . It is thought that long lived organisms actively protect their telomere length 35,36 , and repair their DNA 37,38 .…”
Section: Resultsmentioning
confidence: 99%
“…In addition, telomere sequences were assembled on the ends of most chromosomes, and these telomeres were long compared to other plants with maximum sequences spanning 30 kb as compared to the model plants Arabidopsis thaliana and Zea mays that have 3-5 kb telomeres (Fig. 3b; Supplementary Table 3) 35 . In the Ad77271a genome, we assembled a total of 300 Kb of the ribosomal DNA (rDNA) with only one 26S array that included 35 copies on Chr38, and one 5S array that included 442 copies on Ad77271a Chr01 (Supplementary Table 4).…”
Section: Resultsmentioning
confidence: 99%
“…s 3a; d; e). In general, the centromere arrays assembled well into 1-2 Mb regions that were both metacentric as well as acrocentric (Chr12, 24,26,28,35,38,39 are acrocentric; Supplementary Fig. 9).…”
Section: Baobab Genome Organization: Centromere Telomere Rdna and Dna...mentioning
confidence: 97%
“…In Arabidopsis thaliana, loss of the RPA1B ortholog is sensitive to Ultraviolet B (UV-B) light with reduced chlorophyll A and B and inhibited root growth, which is due to elevated DNA damage 33 . It is thought that long lived organisms actively protect their telomere length 35,36 , and repair their DNA 37,38 . Since the K-mer frequency analysis yielded a haploid genome size of approximately 750 Mb (Table 1) and a graph structure indicative of high heterozygosity ( Fig.…”
Section: Baobab Genome Assembly Annotation and Ploidy Estimationmentioning
Baobab,Adansonia digitata, is a long-lived tree endemic to Africa that holds great economic, ecological, and cultural value. However, our knowledge of its genomic features, evolutionary history, and diversity is limited, rendering it orphaned scientifically. We generated a haploid chromosome-level reference genome anchored into 42 chromosomes forA. digitata, as well as draft assemblies for a sibling tree, two trees from distinct locations in Africa, and a related species,A. zafrom Madagascar. Unlike any other plant to date, DNA transposable elements (TEs) make up 33% of theA. digitatagenome compared to only 10% long terminal repeat retrotransposons (LTR-RTs), which are usually predominant in plant genomes. Baobab has undergone a whole genome duplication (WGD) shared with the Malvoideae ∼30 million years ago (MYA), as well as a confirmed autotetraplody event 3-4 million MYA that coincides with the most recent burst of TE insertions. Resequencing 25A. digitatatrees from Africa revealed three subpopulations that suggest gene flow through most of West Africa but separated from East Africa. Gene enrichment analysis for baobab-specific and high fixation index (Fst) suggested baobab may have retained multiple copies of circadian, light and growth genes to coordinate genome protection for longevity through theUV RESISTANCE LOCUS 8(UVR8) and synchronizing flower development with pollinators. This study lays the groundwork for the creation of breeding resources and the conservation of baobab biodiversity.
“…The HiC connection map suggested the centromere sequence was highly conserved across the chromosomes, and consistent with this, we found a putative centromere repeat with a base unit of 158 bp, and a higher order repeats (HORs) of 314 and 468 bp (Fig.s 3a; d; e). In general, the centromere arrays assembled well into 1-2 Mb regions that were both metacentric as well as acrocentric (Chr12, 24,26,28,35,38,39 are acrocentric; Supplementary Fig. 9).…”
Section: High Dna Transposons Accumulation In Baobab Genomementioning
Baobab, (Adansonia digitata), is a long-lived tree endemic to Africa that holds great economic, ecological, and cultural value. However, our knowledge of its genomic features, evolutionary history, and diversity is limited, rendering it orphaned scientifically. We generated a haploid chromosome-level reference genome anchored into 42 chromosomes for A. digitata, as well as draft assemblies for a sibling tree, two trees from distinct locations in Africa, and a related species, A. za from Madagascar. Unlike any other plant to date, DNA transposable elements (TEs) make up 33% of the A. digitata genome compared to only 10% long terminal repeat retrotransposons (LTR-RTs), which are usually predominant in plant genomes. Baobab has undergone a whole genome duplication (WGD) shared with the Malvoideae ~30 million years ago (MYA), as well as a confirmed autotetraplody event 3-4 million MYA that coincides with the most recent burst of TE insertions. Resequencing 25 A. digitata trees from Africa revealed three subpopulations that suggest gene flow through most of West Africa but separated from East Africa. Gene enrichment analysis for baobab-specific and high fixation index (Fst) suggested baobab may have retained multiple copies of circadian, light and growth genes to coordinate genome protection for longevity through the UV RESISTANCE LOCUS 8 (UVR8) and synchronizing flower development with pollinators. This study lays the groundwork for the creation of breeding resources and the conservation of baobab biodiversity.
Cannabis sativais a globally significant seed-oil, fiber, and drug-producing plant species. However, a century of prohibition has severely restricted legal breeding and germplasm resource development, leaving potential hemp-based nutritional and fiber applications unrealized. Existing cultivars are highly heterozygous and lack competitiveness in the overall fiber and grain markets, relegating hemp to less than 200,000 hectares globally1. The relaxation of drug laws in recent decades has generated widespread interest in expanding and reincorporating cannabis into agricultural systems, but progress has been impeded by the limited understanding of genomics and breeding potential. No studies to date have examined the genomic diversity and evolution of cannabis populations using haplotype-resolved, chromosome-scale assemblies from publicly available germplasm. Here we present a cannabis pangenome, constructed with 181 new and 12 previously released genomes from a total of 156 biological samples from both male (XY) and female (XX) plants, including 42 trio phased and 36 haplotype-resolved, chromosome-scale assemblies. We discovered widespread regions of the cannabis pangenome that are surprisingly diverse for a single species, with high levels of genetic and structural variation, and propose a novel population structure and hybridization history. Conversely, the cannabinoid synthase genes contain very low levels of diversity, despite being embedded within a variable region containing multiple pseudogenized paralogs and distinct transposable element arrangements. Additionally, we identified variants ofacyl-lipid thioesterase (ALT)genes that are associated with fatty acid chain length variation and the production of the rare cannabinoids, tetrahydrocannabinol varin (THCV) and cannabidiol varin (CBDV). We conclude theCannabis sativagene pool has only been partially characterized, and that the existence of wild relatives in Asia remains likely, while its potential as a crop species remains largely unrealized.
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