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1.
Mol Oral Microbiol ; 27(3): 182-201, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22520388

ABSTRACT

High throughput sequencing of 16S ribosomal RNA gene amplicons is a cost-effective method for characterization of oral bacterial communities. However, before undertaking large-scale studies, it is necessary to understand the technique-associated limitations and intrinsic variability of the oral ecosystem. In this work we evaluated bias in species representation using an in vitro-assembled mock community of oral bacteria. We then characterized the bacterial communities in saliva and buccal mucosa of five healthy subjects to investigate the power of high throughput sequencing in revealing their diversity and biogeography patterns. Mock community analysis showed primer and DNA isolation biases and an overestimation of diversity that was reduced after eliminating singleton operational taxonomic units (OTUs). Sequencing of salivary and mucosal communities found a total of 455 OTUs (0.3% dissimilarity) with only 78 of these present in all subjects. We demonstrate that this variability was partly the result of incomplete richness coverage even at great sequencing depths, and so comparing communities by their structure was more effective than comparisons based solely on membership. With respect to oral biogeography, we found inter-subject variability in community structure was lower than site differences between salivary and mucosal communities within subjects. These differences were evident at very low sequencing depths and were mostly caused by the abundance of Streptococcus mitis and Gemella haemolysans in mucosa. In summary, we present an experimental and data analysis framework that will facilitate design and interpretation of pyrosequencing-based studies. Despite challenges associated with this technique, we demonstrate its power for evaluation of oral diversity and biogeography patterns.


Subject(s)
Bacteria/classification , High-Throughput Nucleotide Sequencing/methods , Mouth/microbiology , RNA, Bacterial/analysis , Sequence Analysis, RNA , Actinomyces/classification , Bacteria/genetics , Bias , Biodiversity , DNA, Bacterial/analysis , Fusobacterium nucleatum/classification , Humans , Lacticaseibacillus casei/classification , Metagenome/genetics , Mouth Mucosa/microbiology , Porphyromonas gingivalis/classification , RNA, Ribosomal, 16S/analysis , Saliva/microbiology , Staphylococcaceae/classification , Streptococcus mitis/classification , Streptococcus mutans/classification , Streptococcus oralis/classification , Veillonella/classification , Young Adult
2.
Mamm Genome ; 21(1-2): 77-87, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20033182

ABSTRACT

Multiple Genome Rearrangement (MGR) analysis was used to define the trajectory and pattern of chromosome rearrangement within muroid rodents. MGR was applied using 107 chromosome homologies between Mus, Rattus, Peromyscus, the muroid sister taxon Cricetulus griseus, and Sciurus carolinensis as a non-Muroidea outgroup, with specific attention paid to breakpoint reuse and centromere evolution. This analysis revealed a high level of chromosome breakpoint conservation between Rattus and Peromyscus and indicated that the chromosomes of Mus are highly derived. This analysis identified several conserved evolutionary breakpoints that have been reused multiple times during karyotypic evolution in rodents. Our data demonstrate a high level of reuse of breakpoints among muroid rodents, further supporting the "Fragile Breakage Model" of chromosome evolution. We provide the first analysis of rodent centromeres with respect to evolutionary breakpoints. By analyzing closely related rodent species we were able to clarify muroid rodent karyotypic evolution. We were also able to derive several high-resolution ancestral karyotypes and identify rearrangements specific to various stages of Muroidea evolution. These data were useful in further characterizing lineage-specific modes of chromosome evolution.


Subject(s)
Chromosome Breakpoints , Chromosomes, Mammalian/genetics , Cricetulus/genetics , Peromyscus/genetics , Animals , Biological Evolution , Centromere/genetics , Cricetinae , Gene Rearrangement , Karyotyping , Mice , Phylogeny , Rats , Sciuridae/genetics
3.
Cytogenet Genome Res ; 121(3-4): 288-92, 2008.
Article in English | MEDLINE | ID: mdl-18758174

ABSTRACT

The Mus musculus and Rattus norvegicus genomes have been extensively studied, yet despite the emergence of Peromyscus maniculatus as an NIH model for genome sequencing and biomedical research much remains unknown about the genome organization of Peromyscines. Contrary to their phylogenetic relationship, the genomes of Rattus and Peromyscus appear more similar at the gross karyotypic level than either does to Mus. We set out to define the chromosome homologies between Peromyscus, Mus and Rattus. Reciprocal cross-species chromosome painting and G-band homology assignments were used to delineate the conserved chromosome homology map between P. maniculatus and M. musculus. These data show that each species has undergone extensive chromosome rearrangements since they last shared a common ancestor 25 million years ago (mya). This analysis coupled with an inferred homology map with Rattus revealed a high level of chromosome conservation between Rattus and Peromyscus and indicated that the chromosomes of Mus are highly derived.


Subject(s)
Chromosome Mapping , Chromosome Painting , Mice/genetics , Peromyscus/genetics , Animals , Cells, Cultured , Species Specificity
4.
Cytogenet Genome Res ; 116(1-2): 130-1, 2007.
Article in English | MEDLINE | ID: mdl-17268191

ABSTRACT

The South American opossum Monodelphis domestica has been a model organism for marsupials for many years and has recently been the subject of a large-scale genome sequencing effort that will provide the foundation for comparative studies of gene function and regulation. Genomic imprinting is one mechanism of gene regulation that has received increasing attention due to the impact of imprinting defects on development and disease. We have mapped the imprinted insulin-like growth factor II (IGF2) gene of M. domestica as a first step in understanding the regulatory mechanisms involved in genomic imprinting in this marsupial.


Subject(s)
Genomic Imprinting , Insulin-Like Growth Factor II/genetics , Physical Chromosome Mapping , Animals , Chromosome Mapping , Fibroblasts/metabolism , Gene Library , Genome , In Situ Hybridization, Fluorescence , Insulin/metabolism , Male , Monodelphis
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