@article{
 title = {CRISPR-Cas systems target a diverse collection of invasive mobile genetic elements in human microbiomes},
 type = {article},
 year = {2013},
 keywords = {Bacteria,CRISPR Cas system,CRISPR-Cas Systems,Genes,Humans,Interspersed Repetitive Sequen,Microbial,bacteriophage,feces,human,jo},
 volume = {14},
 websites = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84876800205&doi=10.1186%2Fgb-2013-14-4-r40&partnerID=40&md5=df73488fce6b2a1762b9a99d32d39189},
 publisher = {BioMed Central Ltd.},
 id = {ac3801a7-d06b-33fe-90d9-29c9ab1d8e12},
 created = {2019-10-01T17:20:34.594Z},
 file_attached = {false},
 profile_id = {42d295c0-0737-38d6-8b43-508cab6ea85d},
 last_modified = {2019-10-01T17:24:54.265Z},
 read = {false},
 starred = {false},
 authored = {true},
 confirmed = {true},
 hidden = {false},
 citation_key = {Zhang2013},
 source_type = {article},
 notes = {cited By 16},
 folder_uuids = {b4e18ac7-7050-4c86-a2a4-a9c35bdc74d4},
 private_publication = {false},
 abstract = {Background: Bacteria and archaea develop immunity against invading genomes by incorporating pieces of the invaders' sequences, called spacers, into a clustered regularly interspaced short palindromic repeats (CRISPR) locus between repeats, forming arrays of repeat-spacer units. When spacers are expressed, they direct CRISPR-associated (Cas) proteins to silence complementary invading DNA. In order to characterize the invaders of human microbiomes, we use spacers from CRISPR arrays that we had previously assembled from shotgun metagenomic datasets, and identify contigs that contain these spacers' targets. Results: We discover 95,000 contigs that are putative invasive mobile genetic elements, some targeted by hundreds of CRISPR spacers. We find that oral sites in healthy human populations have a much greater variety of mobile genetic elements than stool samples. Mobile genetic elements carry genes encoding diverse functions: only 7% of the mobile genetic elements are similar to known phages or plasmids, although a much greater proportion contain phage- or plasmid-related genes. A small number of contigs share similarity with known integrative and conjugative elements, providing the first examples of CRISPR defenses against this class of element. We provide detailed analyses of a few large mobile genetic elements of various types, and a relative abundance analysis of mobile genetic elements and putative hosts, exploring the dynamic activities of mobile genetic elements in human microbiomes. A joint analysis of mobile genetic elements and CRISPRs shows that protospacer-adjacent motifs drive their interaction network; however, some CRISPR-Cas systems target mobile genetic elements lacking motifs. Conclusions: We identify a large collection of invasive mobile genetic elements in human microbiomes, an important resource for further study of the interaction between the CRISPR-Cas immune system and invaders. © 2013 BioMed Central Ltd.},
 bibtype = {article},
 author = {Zhang, Q and Rho, M and Tang, H and Doak, T G and Ye, Y},
 doi = {10.1186/gb-2013-14-4-r40},
 journal = {Genome Biology},
 number = {4}
}

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When spacers are expressed, they direct CRISPR-associated (Cas) proteins to silence complementary invading DNA. In order to characterize the invaders of human microbiomes, we use spacers from CRISPR arrays that we had previously assembled from shotgun metagenomic datasets, and identify contigs that contain these spacers' targets. Results: We discover 95,000 contigs that are putative invasive mobile genetic elements, some targeted by hundreds of CRISPR spacers. We find that oral sites in healthy human populations have a much greater variety of mobile genetic elements than stool samples. Mobile genetic elements carry genes encoding diverse functions: only 7% of the mobile genetic elements are similar to known phages or plasmids, although a much greater proportion contain phage- or plasmid-related genes. A small number of contigs share similarity with known integrative and conjugative elements, providing the first examples of CRISPR defenses against this class of element. We provide detailed analyses of a few large mobile genetic elements of various types, and a relative abundance analysis of mobile genetic elements and putative hosts, exploring the dynamic activities of mobile genetic elements in human microbiomes. A joint analysis of mobile genetic elements and CRISPRs shows that protospacer-adjacent motifs drive their interaction network; however, some CRISPR-Cas systems target mobile genetic elements lacking motifs. Conclusions: We identify a large collection of invasive mobile genetic elements in human microbiomes, an important resource for further study of the interaction between the CRISPR-Cas immune system and invaders. © 2013 BioMed Central Ltd.","bibtype":"article","author":"Zhang, Q and Rho, M and Tang, H and Doak, T G and Ye, Y","doi":"10.1186/gb-2013-14-4-r40","journal":"Genome Biology","number":"4","bibtex":"@article{\n title = {CRISPR-Cas systems target a diverse collection of invasive mobile genetic elements in human microbiomes},\n type = {article},\n year = {2013},\n keywords = {Bacteria,CRISPR Cas system,CRISPR-Cas Systems,Genes,Humans,Interspersed Repetitive Sequen,Microbial,bacteriophage,feces,human,jo},\n volume = {14},\n websites = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84876800205&doi=10.1186%2Fgb-2013-14-4-r40&partnerID=40&md5=df73488fce6b2a1762b9a99d32d39189},\n publisher = {BioMed Central Ltd.},\n id = {ac3801a7-d06b-33fe-90d9-29c9ab1d8e12},\n created = {2019-10-01T17:20:34.594Z},\n file_attached = {false},\n profile_id = {42d295c0-0737-38d6-8b43-508cab6ea85d},\n last_modified = {2019-10-01T17:24:54.265Z},\n read = {false},\n starred = {false},\n authored = {true},\n confirmed = {true},\n hidden = {false},\n citation_key = {Zhang2013},\n source_type = {article},\n notes = {cited By 16},\n folder_uuids = {b4e18ac7-7050-4c86-a2a4-a9c35bdc74d4},\n private_publication = {false},\n abstract = {Background: Bacteria and archaea develop immunity against invading genomes by incorporating pieces of the invaders' sequences, called spacers, into a clustered regularly interspaced short palindromic repeats (CRISPR) locus between repeats, forming arrays of repeat-spacer units. 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