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Genome analysis of five recently described species of the CUG-Ser clade uncovers Candida theae as a new hybrid lineage with pathogenic potential in the Candida parapsilosis species complex 对最近描述的五个CUG-Ser分支的基因组分析揭示了假丝酵母菌在假丝酵母菌种复合体中作为一个具有致病潜力的新杂交谱系
IF 4.1 2区 生物学
DNA Research Pub Date : 2022-04-01 DOI: 10.1093/dnares/dsac010
V. Mixão, Valentina del Olmo, Eva Hegedűsová, E. Saus, Leszek P. Pryszcz, Andrea Cillingová, J. Nosek, T. Gabaldón
{"title":"Genome analysis of five recently described species of the CUG-Ser clade uncovers Candida theae as a new hybrid lineage with pathogenic potential in the Candida parapsilosis species complex","authors":"V. Mixão, Valentina del Olmo, Eva Hegedűsová, E. Saus, Leszek P. Pryszcz, Andrea Cillingová, J. Nosek, T. Gabaldón","doi":"10.1093/dnares/dsac010","DOIUrl":"https://doi.org/10.1093/dnares/dsac010","url":null,"abstract":"Abstract Candida parapsilosis species complex comprises three important pathogenic species: Candida parapsilosis sensu stricto, Candida orthopsilosis and Candida metapsilosis. The majority of C. orthopsilosis and all C. metapsilosis isolates sequenced thus far are hybrids, and most of the parental lineages remain unidentified. This led to the hypothesis that hybrids with pathogenic potential were formed by the hybridization of non-pathogenic lineages that thrive in the environment. In a search for the missing hybrid parentals, and aiming to get a better understanding of the evolution of the species complex, we sequenced, assembled and analysed the genome of five close relatives isolated from the environment: Candida jiufengensis, Candida pseudojiufengensis, Candida oxycetoniae, Candida margitis and Candida theae. We found that the linear conformation of mitochondrial genomes in Candida species emerged multiple times independently. Furthermore, our analyses discarded the possible involvement of these species in the mentioned hybridizations, but identified C. theae as an additional hybrid in the species complex. Importantly, C. theae was recently associated with a case of infection, and we also uncovered the hybrid nature of this clinical isolate. Altogether, our results reinforce the hypothesis that hybridization is widespread among Candida species, and potentially contributes to the emergence of lineages with opportunistic pathogenic behaviour.","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"29 1","pages":""},"PeriodicalIF":4.1,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"61096972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Chromosomal-level genome assembly of the orchid tree Bauhinia variegata (Leguminosae; Cercidoideae) supports the allotetraploid origin hypothesis of Bauhinia 兰树紫荆(bahinia variegata)染色体水平基因组组装的研究支持紫荆属异源四倍体起源假说
IF 4.1 2区 生物学
DNA Research Pub Date : 2022-04-01 DOI: 10.1093/dnares/dsac012
Y. Zhong, Yong Chen, Danjing Zheng, Jingyi Pang, Ying Liu, Shukai Luo, Shi-hua Meng, Lei Qian, Dan Wei, S. Dai, R. Zhou
{"title":"Chromosomal-level genome assembly of the orchid tree Bauhinia variegata (Leguminosae; Cercidoideae) supports the allotetraploid origin hypothesis of Bauhinia","authors":"Y. Zhong, Yong Chen, Danjing Zheng, Jingyi Pang, Ying Liu, Shukai Luo, Shi-hua Meng, Lei Qian, Dan Wei, S. Dai, R. Zhou","doi":"10.1093/dnares/dsac012","DOIUrl":"https://doi.org/10.1093/dnares/dsac012","url":null,"abstract":"Abstract Cercidoideae, one of the six subfamilies of Leguminosae, contains one genus Cercis with its chromosome number 2n = 14 and all other genera with 2n = 28. An allotetraploid origin hypothesis for the common ancestor of non-Cercis genera in this subfamily has been proposed; however, no chromosome-level genomes from Cercidoideae have been available to test this hypothesis. Here, we conducted a chromosome-level genome assembly of Bauhinia variegata to test this hypothesis. The assembled genome is 326.4 Mb with the scaffold N50 of 22.1 Mb and contains 37,996 protein-coding genes. The Ks distribution between gene pairs in the syntenic regions indicates two whole-genome duplications (WGDs): one is B. variegata-specific, and the other is shared among core eudicots. Although Ks between gene pairs generated by the recent WGD in Bauhinia is greater than that between Bauhinia and Cercis, the WGD was not detected in Cercis, which can be explained by an accelerated evolutionary rate in Bauhinia after divergence from Cercis. Ks distribution and phylogenetic analysis for gene pairs generated by the recent WGD in Bauhinia and their corresponding orthologs in Cercis support the allopolyploidy origin hypothesis of Bauhinia. The genome of B. variegata also provides a genomic resource for dissecting genetic basis of its ornamental traits.","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"10 1","pages":""},"PeriodicalIF":4.1,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"61097063","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Chromosome-level genome assembly of a xerophytic plant, Haloxylon ammodendron. 一种旱生植物梭梭的染色体水平基因组组装。
IF 4.1 2区 生物学
DNA Research Pub Date : 2022-02-27 DOI: 10.1093/dnares/dsac006
Mingcheng Wang, Lei Zhang, Shaofei Tong, Dechun Jiang, Zhixi Fu
{"title":"Chromosome-level genome assembly of a xerophytic plant, Haloxylon ammodendron.","authors":"Mingcheng Wang,&nbsp;Lei Zhang,&nbsp;Shaofei Tong,&nbsp;Dechun Jiang,&nbsp;Zhixi Fu","doi":"10.1093/dnares/dsac006","DOIUrl":"https://doi.org/10.1093/dnares/dsac006","url":null,"abstract":"<p><p>Haloxylon ammodendron is a xerophytic perennial shrub or small tree that has a high ecological value in anti-desertification due to its high tolerance to drought and salt stress. Here, we report a high-quality, chromosome-level genome assembly of H. ammodendron by integrating PacBio's high-fidelity sequencing and Hi-C technology. The assembled genome size was 685.4 Mb, of which 99.6% was assigned to nine pseudochromosomes with a contig N50 value of 23.6 Mb. Evolutionary analysis showed that both the recent substantial amplification of long terminal repeat retrotransposons and tandem gene duplication may have contributed to its genome size expansion and arid adaptation. An ample amount of low-GC genes was closely related to functions that may contribute to the desert adaptation of H. ammodendron. Gene family clustering together with gene expression analysis identified differentially expressed genes that may play important roles in the direct response of H. ammodendron to water-deficit stress. We also identified several genes possibly related to the degraded scaly leaves and well-developed root system of H. ammodendron. The reference-level genome assembly presented here will provide a valuable genomic resource for studying the genome evolution of xerophytic plants, as well as for further genetic breeding studies of H. ammodendron.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"29 2","pages":""},"PeriodicalIF":4.1,"publicationDate":"2022-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946665/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71428849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
A chromosome-scale genome and transcriptomic analysis of the endangered tropical tree Vatica mangachapoi (Dipterocarpaceae). 濒危热带树Vatica mangachapoi的染色体尺度基因组和转录组学分析。
IF 4.1 2区 生物学
DNA Research Pub Date : 2022-02-27 DOI: 10.1093/dnares/dsac005
Liang Tang, Xuezhu Liao, Luke R Tembrock, Song Ge, Zhiqiang Wu
{"title":"A chromosome-scale genome and transcriptomic analysis of the endangered tropical tree Vatica mangachapoi (Dipterocarpaceae).","authors":"Liang Tang,&nbsp;Xuezhu Liao,&nbsp;Luke R Tembrock,&nbsp;Song Ge,&nbsp;Zhiqiang Wu","doi":"10.1093/dnares/dsac005","DOIUrl":"https://doi.org/10.1093/dnares/dsac005","url":null,"abstract":"<p><p>Vatica mangachapoi is a tropical tree species native to Southeast Asia. It has long been valued as a timber species because the wood resists decay, but it is now considered vulnerable to extinction due to habitat loss and overexploitation. Here, we present the first chromosome-level genome assembly of V. mangachapoi that we created by combining data from PacBio long read sequencing with Hi-C proximity ligation and Illumina short-read sequencing. The assembled genome was 456.21 Mb, containing 11 chromosome and a BUSCO score of 93.4%. From the newly assembled genome, 46,811 protein-coding genes were predicted. Repetitive DNA accounted for 53% of the genome. Phylogenomic and gene family analyses showed that V. mangachapoi diverged from a common ancestor of Gossypium raimondii 70 million years ago. Transcriptome analyses found 227 genes that were differentially expressed in the leaves of plants grown in normal soil relative to plants grown in dry, coastal, sandy soil. For these genes, we identified three significantly enriched with GO terms: responses to organonitrogen compounds, chitin-triggered immunity, and wound response. This genome provides an important comparative benchmark not only for future conservation work on V. mangachapoi but also for phylogenomics work on Dipterocarpaceae.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"29 2","pages":""},"PeriodicalIF":4.1,"publicationDate":"2022-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882376/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39790271","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Chromosome-scale assembly of barley cv. 'Haruna Nijo' as a resource for barley genetics. 大麦cv的染色体规模组装。“二条春菜”作为大麦遗传资源。
IF 4.1 2区 生物学
DNA Research Pub Date : 2022-01-28 DOI: 10.1093/dnares/dsac001
Areej Sakkour, Martin Mascher, Axel Himmelbach, Georg Haberer, Thomas Lux, Manuel Spannagl, Nils Stein, Shoko Kawamoto, Kazuhiro Sato
{"title":"Chromosome-scale assembly of barley cv. 'Haruna Nijo' as a resource for barley genetics.","authors":"Areej Sakkour,&nbsp;Martin Mascher,&nbsp;Axel Himmelbach,&nbsp;Georg Haberer,&nbsp;Thomas Lux,&nbsp;Manuel Spannagl,&nbsp;Nils Stein,&nbsp;Shoko Kawamoto,&nbsp;Kazuhiro Sato","doi":"10.1093/dnares/dsac001","DOIUrl":"https://doi.org/10.1093/dnares/dsac001","url":null,"abstract":"<p><p>Cultivated barley (Hordeum vulgare ssp. vulgare) is used for food, animal feed, and alcoholic beverages and is widely grown in temperate regions. Both barley and its wild progenitor (H. vulgare ssp. spontaneum) have large 5.1-Gb genomes. High-quality chromosome-scale assemblies for several representative barley genotypes, both wild and domesticated, have been constructed recently to populate the nascent barley pan-genome infrastructure. Here, we release a chromosome-scale assembly of the Japanese elite malting barley cultivar 'Haruna Nijo' using a similar methodology as in the barley pan-genome project. The 4.28-Gb assembly had a scaffold N50 size of 18.9 Mb. The assembly showed high collinearity with the barley reference genome 'Morex' cultivar, with some inversions. The pseudomolecule assembly was characterized using transcript evidence of gene projection derived from the reference genome and de novo gene annotation achieved using published full-length cDNA sequences and RNA-Seq data for 'Haruna Nijo'. We found good concordance between our whole-genome assembly and the publicly available BAC clone sequence of 'Haruna Nijo'. Interesting phenotypes have since been identified in Haruna Nijo; its genome sequence assembly will facilitate the identification of the underlying genes.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"29 1","pages":""},"PeriodicalIF":4.1,"publicationDate":"2022-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798153/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10246920","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Erratum to: Long-read metagenomics of multiple displacement amplified DNA of low-biomass human gut phageomes by SACRA pre-processing chimeric reads. 通过SACRA预处理嵌合reads对低生物量人类肠道噬菌体的多位移扩增DNA进行长读宏基因组学校正。
IF 4.1 2区 生物学
DNA Research Pub Date : 2021-10-11 DOI: 10.1093/dnares/dsab025
Yuya Kiguchi, Suguru Nishijima, Naveen Kumar, Masahira Hattori, Wataru Suda
{"title":"Erratum to: Long-read metagenomics of multiple displacement amplified DNA of low-biomass human gut phageomes by SACRA pre-processing chimeric reads.","authors":"Yuya Kiguchi,&nbsp;Suguru Nishijima,&nbsp;Naveen Kumar,&nbsp;Masahira Hattori,&nbsp;Wataru Suda","doi":"10.1093/dnares/dsab025","DOIUrl":"https://doi.org/10.1093/dnares/dsab025","url":null,"abstract":"Erratum to: Long-read metagenomics of multiple displacement amplified DNA of low-biomass human gut phageomes by SACRA pre-processing chimeric reads Yuya Kiguchi , Suguru Nishijima, Naveen Kumar, Masahira Hattori*, and Wataru Suda* Cooperative Major in Advanced Health Science, Graduate School of Advanced Science and Engineering, Waseda University, Tokyo 169-8555, Japan, Computational Bio Big-Data Open Innovation Laboratory (CBBD-OIL), National Institute of Advanced Industrial Science and Technology, Tokyo 169-8555, Japan, Laboratory for Microbiome Sciences, RIKEN Center for Integrative Medical Sciences, Yokohama 230-0045, Japan, Integrated Institute for Regulatory Science, Waseda University, Tokyo 169-8555, Japan, and Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"28 6","pages":""},"PeriodicalIF":4.1,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/75/cc/dsab025.PMC8660067.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39707018","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-read metagenomics of multiple displacement amplified DNA of low-biomass human gut phageomes by SACRA pre-processing chimeric reads. 通过SACRA预处理嵌合reads对低生物量人肠道噬菌体多位移扩增DNA进行长读宏基因组学研究。
IF 4.1 2区 生物学
DNA Research Pub Date : 2021-10-11 DOI: 10.1093/dnares/dsab019
Yuya Kiguchi, Suguru Nishijima, Naveen Kumar, Masahira Hattori, Wataru Suda
{"title":"Long-read metagenomics of multiple displacement amplified DNA of low-biomass human gut phageomes by SACRA pre-processing chimeric reads.","authors":"Yuya Kiguchi,&nbsp;Suguru Nishijima,&nbsp;Naveen Kumar,&nbsp;Masahira Hattori,&nbsp;Wataru Suda","doi":"10.1093/dnares/dsab019","DOIUrl":"https://doi.org/10.1093/dnares/dsab019","url":null,"abstract":"<p><p>The human gut bacteriophage community (phageome) plays an important role in the host's health and disease; however, the entire structure is poorly understood, partly owing to the generation of many incomplete genomes in conventional short-read metagenomics. Here, we show long-read metagenomics of amplified DNA of low-biomass phageomes with multiple displacement amplification (MDA), involving the development of a novel bioinformatics tool, split amplified chimeric read algorithm (SACRA), that efficiently pre-processed numerous chimeric reads generated through MDA. Using five samples, SACRA markedly reduced the average chimera ratio from 72% to 1.5% in PacBio reads with an average length of 1.8 kb. De novo assembly of chimera-less PacBio long reads reconstructed contigs of ≥5 kb with an average proportion of 27%, which was 1% in contigs from MiSeq short reads, thereby dramatically improving contig length and genome completeness. Comparison of PacBio and MiSeq contigs found MiSeq contig fragmentations frequently near local repeats and hypervariable regions in the phage genomes, and those caused by multiple homologous phage genomes coexisting in the community. We also developed a reference-independent method to assess the completeness of the linear phage genomes. Overall, we established a SACRA-coupled long-read metagenomics robust to highly diverse gut phageomes, identifying high-quality circular and linear phage genomes with adequate sequence quantity.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"28 6","pages":""},"PeriodicalIF":4.1,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8513251/pdf/dsab019.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39468401","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Genome-wide simple sequence repeat markers in potato: abundance, distribution, composition, and polymorphism. 马铃薯全基因组简单序列重复标记:丰度、分布、组成和多态性。
IF 4.1 2区 生物学
DNA Research Pub Date : 2021-10-11 DOI: 10.1093/dnares/dsab020
Yinqiao Jian, Wenyuan Yan, Jianfei Xu, Shaoguang Duan, Guangcun Li, Liping Jin
{"title":"Genome-wide simple sequence repeat markers in potato: abundance, distribution, composition, and polymorphism.","authors":"Yinqiao Jian,&nbsp;Wenyuan Yan,&nbsp;Jianfei Xu,&nbsp;Shaoguang Duan,&nbsp;Guangcun Li,&nbsp;Liping Jin","doi":"10.1093/dnares/dsab020","DOIUrl":"https://doi.org/10.1093/dnares/dsab020","url":null,"abstract":"<p><p>Simple sequence repeats (SSRs) are important sources of genetic diversity and are widely used as markers in genetics and molecular breeding. In this study, we examined four potato genomes of DM1-3 516 R44 (DM) from Solanum phureja, RH89039-16 (RH) from Solanum tuberosum, M6 from Solanum chacoense and Solanum commersonii to determine SSR abundance and distribution and develop a larger list of polymorphic markers for a potentially wide range of uses for the potato community. A total of 1,734,619 SSRs were identified across the four genomes with an average of 433,655 SSRs per genome and 2.31kb per SSR. The most abundant repeat units for mono-, di-, tri-, and tetra-nucleotide SSRs were (A/T)n, (AT/AT)n, (AAT/ATT)n, and (ATAT/ATAT)n, respectively. The SSRs were most abundant (78.79%) in intergenic regions and least abundant (3.68%) in untranslated regions. On average, 168,069 SSRs with unique flanking sequences were identified in the four genomes. Further, we identified 16,245 polymorphic SSR markers among the four genomes. Experimental validation confirmed 99.69% of tested markers could generate target bands. The high-density potato SSR markers developed in this study will undoubtedly facilitate the application of SSR markers for genetic research and marker-pyramiding in potato breeding.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"28 6","pages":""},"PeriodicalIF":4.1,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641542/pdf/dsab020.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39486345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Genome sequencing of the NIES Cyanobacteria collection with a focus on the heterocyst-forming clade. 对 NIES 蓝藻菌群进行基因组测序,重点关注杂囊形成支系。
IF 3.9 2区 生物学
DNA Research Pub Date : 2021-10-11 DOI: 10.1093/dnares/dsab024
Yuu Hirose, Yoshiyuki Ohtsubo, Naomi Misawa, Chinatsu Yonekawa, Nobuyoshi Nagao, Yohei Shimura, Takatomo Fujisawa, Yu Kanesaki, Hiroshi Katoh, Mitsunori Katayama, Haruyo Yamaguchi, Hirofumi Yoshikawa, Masahiko Ikeuchi, Toshihiko Eki, Yasukazu Nakamura, Masanobu Kawachi
{"title":"Genome sequencing of the NIES Cyanobacteria collection with a focus on the heterocyst-forming clade.","authors":"Yuu Hirose, Yoshiyuki Ohtsubo, Naomi Misawa, Chinatsu Yonekawa, Nobuyoshi Nagao, Yohei Shimura, Takatomo Fujisawa, Yu Kanesaki, Hiroshi Katoh, Mitsunori Katayama, Haruyo Yamaguchi, Hirofumi Yoshikawa, Masahiko Ikeuchi, Toshihiko Eki, Yasukazu Nakamura, Masanobu Kawachi","doi":"10.1093/dnares/dsab024","DOIUrl":"10.1093/dnares/dsab024","url":null,"abstract":"<p><p>Cyanobacteria are a diverse group of Gram-negative prokaryotes that perform oxygenic photosynthesis. Cyanobacteria have been used for research on photosynthesis and have attracted attention as a platform for biomaterial/biofuel production. Cyanobacteria are also present in almost all habitats on Earth and have extensive impacts on global ecosystems. Given their biological, economical, and ecological importance, the number of high-quality genome sequences for Cyanobacteria strains is limited. Here, we performed genome sequencing of Cyanobacteria strains in the National Institute for Environmental Studies microbial culture collection in Japan. We sequenced 28 strains that can form a heterocyst, a morphologically distinct cell that is specialized for fixing nitrogen, and 3 non-heterocystous strains. Using Illumina sequencing of paired-end and mate-pair libraries with in silico finishing, we constructed highly contiguous assemblies. We determined the phylogenetic relationship of the sequenced genome assemblies and found potential difficulties in the classification of certain heterocystous clades based on morphological observation. We also revealed a bias on the sequenced strains by the phylogenetic analysis of the 16S rRNA gene including unsequenced strains. Genome sequencing of Cyanobacteria strains deposited in worldwide culture collections will contribute to understanding the enormous genetic and phenotypic diversity within the phylum Cyanobacteria.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"28 6","pages":""},"PeriodicalIF":3.9,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39566207","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genome sequencing and analysis of two early-flowering cherry (Cerasus × kanzakura) varieties, 'Kawazu-zakura' and 'Atami-zakura'. 两个早花樱桃(Cerasus × kanzakura)品种‘Kawazu-zakura’和‘Atami-zakura’的基因组测序和分析。
IF 4.1 2区 生物学
DNA Research Pub Date : 2021-10-11 DOI: 10.1093/dnares/dsab026
Kenta Shirasawa, Akihiro Itai, Sachiko Isobe
{"title":"Genome sequencing and analysis of two early-flowering cherry (Cerasus × kanzakura) varieties, 'Kawazu-zakura' and 'Atami-zakura'.","authors":"Kenta Shirasawa,&nbsp;Akihiro Itai,&nbsp;Sachiko Isobe","doi":"10.1093/dnares/dsab026","DOIUrl":"https://doi.org/10.1093/dnares/dsab026","url":null,"abstract":"<p><p>To gain genetic insights into the early-flowering phenotype of ornamental cherry, also known as sakura, we determined the genome sequences of two early-flowering cherry (Cerasus × kanzakura) varieties, 'Kawazu-zakura' and 'Atami-zakura'. Because the two varieties are interspecific hybrids, likely derived from crosses between Cerasus campanulata (early-flowering species) and Cerasus speciosa, we employed the haplotype-resolved sequence assembly strategy. Genome sequence reads obtained from each variety by single-molecule real-time sequencing (SMRT) were split into two subsets, based on the genome sequence information of the two probable ancestors, and assembled to obtain haplotype-phased genome sequences. The resultant genome assembly of 'Kawazu-zakura' spanned 519.8 Mb with 1,544 contigs and an N50 value of 1,220.5 kb, while that of 'Atami-zakura' totalled 509.6 Mb with 2,180 contigs and an N50 value of 709.1 kb. A total of 72,702 and 69,528 potential protein-coding genes were predicted in the genome assemblies of 'Kawazu-zakura' and 'Atami-zakura', respectively. Gene clustering analysis identified 2,634 clusters uniquely presented in the C. campanulata haplotype sequences, which might contribute to its early-flowering phenotype. Genome sequences determined in this study provide fundamental information for elucidating the molecular and genetic mechanisms underlying the early-flowering phenotype of ornamental cherry tree varieties and their relatives.</p>","PeriodicalId":51014,"journal":{"name":"DNA Research","volume":"28 6","pages":""},"PeriodicalIF":4.1,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643691/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39635411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
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