Abstract:We performed whole-genome resequencing of 12 field isolates and eight commonly studied laboratory strains of the model organism Chlamydomonas reinhardtii to characterize genomic diversity and provide a resource for studies of natural variation. Our data support previous observations that Chlamydomonas is among the most diverse eukaryotic species. Nucleotide diversity is ;3% and is geographically structured in North America with some evidence of admixture among sampling locales. Examination of predicted loss-of… Show more
“…However, it is interesting to note that the rate of variants within these blocks, 2.0%, was comparable to the 2.4% rate of variation that we observed in CC-2290, as well as the 2.83% average variant rate for wild isolates of Chlamydomonas as reported by Flowers et al (2015). (A) Identification of variants.…”
Section: The Genomes Of the Chlamydomonas Standard Laboratory Strainssupporting
confidence: 85%
“…In work cosubmitted with this article, Flowers et al (2015) also observed ways in which mutations present in the sequenced strains of Chlamydomonas were biased toward those that are less deleterious to gene expression. For example, they observed that 28% of genes with premature stop codons encode proteins that are truncated by 5% or less.…”
Section: Effects Of Haplotype 2 On Genesmentioning
Chlamydomonas reinhardtii is a widely used reference organism in studies of photosynthesis, cilia, and biofuels. Most research in this field uses a few dozen standard laboratory strains that are reported to share a common ancestry, but exhibit substantial phenotypic differences. In order to facilitate ongoing Chlamydomonas research and explain the phenotypic variation, we mapped the genetic diversity within these strains using whole-genome resequencing. We identified 524,640 single nucleotide variants and 4812 structural variants among 39 commonly used laboratory strains. Nearly all (98.2%) of the total observed genetic diversity was attributable to the presence of two, previously unrecognized, alternate haplotypes that are distributed in a mosaic pattern among the extant laboratory strains. We propose that these two haplotypes are the remnants of an ancestral cross between two strains with ;2% relative divergence. These haplotype patterns create a fingerprint for each strain that facilitates the positive identification of that strain and reveals its relatedness to other strains. The presence of these alternate haplotype regions affects phenotype scoring and gene expression measurements. Here, we present a rich set of genetic differences as a community resource to allow researchers to more accurately conduct and interpret their experiments with Chlamydomonas.
“…However, it is interesting to note that the rate of variants within these blocks, 2.0%, was comparable to the 2.4% rate of variation that we observed in CC-2290, as well as the 2.83% average variant rate for wild isolates of Chlamydomonas as reported by Flowers et al (2015). (A) Identification of variants.…”
Section: The Genomes Of the Chlamydomonas Standard Laboratory Strainssupporting
confidence: 85%
“…In work cosubmitted with this article, Flowers et al (2015) also observed ways in which mutations present in the sequenced strains of Chlamydomonas were biased toward those that are less deleterious to gene expression. For example, they observed that 28% of genes with premature stop codons encode proteins that are truncated by 5% or less.…”
Section: Effects Of Haplotype 2 On Genesmentioning
Chlamydomonas reinhardtii is a widely used reference organism in studies of photosynthesis, cilia, and biofuels. Most research in this field uses a few dozen standard laboratory strains that are reported to share a common ancestry, but exhibit substantial phenotypic differences. In order to facilitate ongoing Chlamydomonas research and explain the phenotypic variation, we mapped the genetic diversity within these strains using whole-genome resequencing. We identified 524,640 single nucleotide variants and 4812 structural variants among 39 commonly used laboratory strains. Nearly all (98.2%) of the total observed genetic diversity was attributable to the presence of two, previously unrecognized, alternate haplotypes that are distributed in a mosaic pattern among the extant laboratory strains. We propose that these two haplotypes are the remnants of an ancestral cross between two strains with ;2% relative divergence. These haplotype patterns create a fingerprint for each strain that facilitates the positive identification of that strain and reveals its relatedness to other strains. The presence of these alternate haplotype regions affects phenotype scoring and gene expression measurements. Here, we present a rich set of genetic differences as a community resource to allow researchers to more accurately conduct and interpret their experiments with Chlamydomonas.
“…Therefore, during the RNA-seq mapping, we allowed three mismatches after considering average synonymous polymorphism among the field isolates (nucleotide diversity at synonymous sites, dS = 0.0317, Flowers et al, 2015). As a result, mapping rates range between 82.1% and 98.2% of the total reads (Supplemental Table S2).…”
Section: Experimental Design For Identifying Ez-specific Genesmentioning
The sexual cycle of the unicellular Chlamydomonas reinhardtii culminates in the formation of diploid zygotes that differentiate into dormant spores that eventually undergo meiosis. Mating between gametes induces rapid cell wall shedding via the enzyme g-lysin; cell fusion is followed by heterodimerization of sex-specific homeobox transcription factors, GSM1 and GSP1, and initiation of zygote-specific gene expression. To investigate the genetic underpinnings of the zygote developmental pathway, we performed comparative transcriptome analysis of both pre-and post-fertilization samples. We identified 253 transcripts specifically enriched in early zygotes, 82% of which were not up-regulated in gsp1 null zygotes. We also found that the GSM1/GSP1 heterodimer negatively regulates the vegetative wall program at the posttranscriptional level, enabling prompt transition from vegetative wall to zygotic wall assembly. Annotation of the g-lysin-induced and early zygote genes reveals distinct vegetative and zygotic wall programs, supported by concerted up-regulation of genes encoding cell wall-modifying enzymes and proteins involved in nucleotide-sugar metabolism. The haploid-to-diploid transition in Chlamydomonas is masterfully controlled by the GSM1/GSP1 heterodimer, translating fertilization and gamete coalescence into a bona fide differentiation program. The fertilization-triggered integration of genes required to make related, but structurally and functionally distinct organelles-the vegetative versus zygote cell wall-presents a likely scenario for the evolution of complex developmental gene regulatory networks.
“…In a related study of genomic diversity in Chlamydomonas, Flowers et al (2015) used whole-genome resequencing to analyze genetic diversity in 12 field isolates from Phenotypic variation of Chlamydomonas laboratory strains in response to iron concentration (top panel). Geographic clustering of field strains is shown in the bottom panel.…”
mentioning
confidence: 99%
“…Geographic clustering of field strains is shown in the bottom panel. (Reprinted from Gallaher et al [2015], Supplemental Figure 1A, and Flowers et al [2015], Figure 2A. ) www.plantcell.org/cgi/doi/10.1105/tpc.15.00778…”
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.