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Dive into the research topics where Jasmyn Pangilinan is active.

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Featured researches published by Jasmyn Pangilinan.


Science | 2011

The ecoresponsive genome of Daphnia pulex

John K. Colbourne; Michael E. Pfrender; Donald L. Gilbert; W. Kelley Thomas; Abraham Tucker; Todd H. Oakley; Shin-ichi Tokishita; Andrea Aerts; Georg J. Arnold; Malay Kumar Basu; Darren J Bauer; Carla E. Cáceres; Liran Carmel; Claudio Casola; Jeong Hyeon Choi; John C. Detter; Qunfeng Dong; Serge Dusheyko; Brian D. Eads; Thomas Fröhlich; Kerry A. Geiler-Samerotte; Daniel Gerlach; Phil Hatcher; Sanjuro Jogdeo; Jeroen Krijgsveld; Evgenia V. Kriventseva; Dietmar Kültz; Christian Laforsch; Erika Lindquist; Jacqueline Lopez

The Daphnia genome reveals a multitude of genes and shows adaptation through gene family expansions. We describe the draft genome of the microcrustacean Daphnia pulex, which is only 200 megabases and contains at least 30,907 genes. The high gene count is a consequence of an elevated rate of gene duplication resulting in tandem gene clusters. More than a third of Daphnia’s genes have no detectable homologs in any other available proteome, and the most amplified gene families are specific to the Daphnia lineage. The coexpansion of gene families interacting within metabolic pathways suggests that the maintenance of duplicated genes is not random, and the analysis of gene expression under different environmental conditions reveals that numerous paralogs acquire divergent expression patterns soon after duplication. Daphnia-specific genes, including many additional loci within sequenced regions that are otherwise devoid of annotations, are the most responsive genes to ecological challenges.


Nature Biotechnology | 2006

Metagenomic analysis of two enhanced biological phosphorus removal (EBPR) sludge communities

Hector Garcia Martin; Natalia Ivanova; Victor Kunin; Falk Warnecke; Kerrie Barry; Alice C. McHardy; Christine Yeates; Shaomei He; Asaf Salamov; Ernest Szeto; Eileen Dalin; Nik Putnam; Harris Shapiro; Jasmyn Pangilinan; Isidore Rigoutsos; Nikos C. Kyrpides; Linda L. Blackall; Katherine D. McMahon; Philip Hugenholtz

Enhanced biological phosphorus removal (EBPR) is one of the best-studied microbially mediated industrial processes because of its ecological and economic relevance. Despite this, it is not well understood at the metabolic level. Here we present a metagenomic analysis of two lab-scale EBPR sludges dominated by the uncultured bacterium, “Candidatus Accumulibacter phosphatis.” The analysis sheds light on several controversies in EBPR metabolic models and provides hypotheses explaining the dominance of A. phosphatis in this habitat, its lifestyle outside EBPR and probable cultivation requirements. Comparison of the same species from different EBPR sludges highlights recent evolutionary dynamics in the A. phosphatis genome that could be linked to mechanisms for environmental adaptation. In spite of an apparent lack of phylogenetic overlap in the flanking communities of the two sludges studied, common functional themes were found, at least one of them complementary to the inferred metabolism of the dominant organism. The present study provides a much needed blueprint for a systems-level understanding of EBPR and illustrates that metagenomics enables detailed, often novel, insights into even well-studied biological systems.


Science | 2009

Green evolution and dynamic adaptations revealed by genomes of the marine picoeukaryotes Micromonas.

Alexandra Z. Worden; Jae-Hyeok Lee; Thomas Mock; Pierre Rouzé; Melinda P. Simmons; Andrea Aerts; Andrew E. Allen; Marie L. Cuvelier; Evelyne Derelle; Meredith V. Everett; Elodie Foulon; Jane Grimwood; Heidrun Gundlach; Bernard Henrissat; Carolyn A. Napoli; Sarah M. McDonald; Micaela S. Parker; Stephane Rombauts; Aasf Salamov; Peter von Dassow; Jonathan H. Badger; Pedro M. Coutinho; Elif Demir; Inna Dubchak; Chelle Gentemann; Wenche Eikrem; Jill E. Gready; Uwe John; William Lanier; Erika Lindquist

Picoeukaryotes are a taxonomically diverse group of organisms less than 2 micrometers in diameter. Photosynthetic marine picoeukaryotes in the genus Micromonas thrive in ecosystems ranging from tropical to polar and could serve as sentinel organisms for biogeochemical fluxes of modern oceans during climate change. These broadly distributed primary producers belong to an anciently diverged sister clade to land plants. Although Micromonas isolates have high 18S ribosomal RNA gene identity, we found that genomes from two isolates shared only 90% of their predicted genes. Their independent evolutionary paths were emphasized by distinct riboswitch arrangements as well as the discovery of intronic repeat elements in one isolate, and in metagenomic data, but not in other genomes. Divergence appears to have been facilitated by selection and acquisition processes that actively shape the repertoire of genes that are mutually exclusive between the two isolates differently than the core genes. Analyses of the Micromonas genomes offer valuable insights into ecological differentiation and the dynamic nature of early plant evolution.


Science | 2010

Genomic Analysis of Organismal Complexity in the Multicellular Green Alga Volvox carteri

Simon Prochnik; James G. Umen; Aurora M. Nedelcu; Armin Hallmann; Stephen M. Miller; Ichiro Nishii; Patrick J. Ferris; Alan Kuo; Therese Mitros; Lillian K. Fritz-Laylin; Uffe Hellsten; Jarrod Chapman; Oleg Simakov; Stefan A. Rensing; Astrid Terry; Jasmyn Pangilinan; Vladimir V. Kapitonov; Jerzy Jurka; Asaf Salamov; Harris Shapiro; Jeremy Schmutz; Jane Grimwood; Erika Lindquist; Susan Lucas; Igor V. Grigoriev; Rüdiger Schmitt; David L. Kirk; Daniel S. Rokhsar

Going Multicellular The volvocine algae include both the unicellular Chlamydomonas and the multicellular Volvox, which diverged from one another 50 to 200 million years ago. Prochnik et al. (p. 223) compared the Volvox genome with that of Chlamydomonas to identify any genomic innovations that might have been associated with the transition to multicellularity. Size changes were observed in several protein families in Volvox, but, overall, the Volvox genome and predicted proteome were highly similar to those of Chlamydomonas. Thus, biological complexity can arise without major changes in genome content or protein domains. Comparison of the Chlamydomonas and Volvox genomes show few differences, despite their divergent life histories. The multicellular green alga Volvox carteri and its morphologically diverse close relatives (the volvocine algae) are well suited for the investigation of the evolution of multicellularity and development. We sequenced the 138–mega–base pair genome of V. carteri and compared its ~14,500 predicted proteins to those of its unicellular relative Chlamydomonas reinhardtii. Despite fundamental differences in organismal complexity and life history, the two species have similar protein-coding potentials and few species-specific protein-coding gene predictions. Volvox is enriched in volvocine-algal–specific proteins, including those associated with an expanded and highly compartmentalized extracellular matrix. Our analysis shows that increases in organismal complexity can be associated with modifications of lineage-specific proteins rather than large-scale invention of protein-coding capacity.


Proceedings of the National Academy of Sciences of the United States of America | 2011

Obligate biotrophy features unraveled by the genomic analysis of rust fungi

Sébastien Duplessis; Christina A. Cuomo; Yao-Cheng Lin; Andrea Aerts; Emilie Tisserant; Claire Veneault-Fourrey; David L. Joly; Stéphane Hacquard; Joelle Amselem; Brandi L. Cantarel; Readman Chiu; Pedro M. Coutinho; Nicolas Feau; Matthew A. Field; Pascal Frey; Eric Gelhaye; Jonathan M. Goldberg; Manfred Grabherr; Chinnappa D. Kodira; Annegret Kohler; Ursula Kües; Erika Lindquist; Susan Lucas; Rohit Mago; Evan Mauceli; Emmanuelle Morin; Claude Murat; Jasmyn Pangilinan; Robert F. Park; Matthew Pearson

Rust fungi are some of the most devastating pathogens of crop plants. They are obligate biotrophs, which extract nutrients only from living plant tissues and cannot grow apart from their hosts. Their lifestyle has slowed the dissection of molecular mechanisms underlying host invasion and avoidance or suppression of plant innate immunity. We sequenced the 101-Mb genome of Melampsora larici-populina, the causal agent of poplar leaf rust, and the 89-Mb genome of Puccinia graminis f. sp. tritici, the causal agent of wheat and barley stem rust. We then compared the 16,399 predicted proteins of M. larici-populina with the 17,773 predicted proteins of P. graminis f. sp tritici. Genomic features related to their obligate biotrophic lifestyle include expanded lineage-specific gene families, a large repertoire of effector-like small secreted proteins, impaired nitrogen and sulfur assimilation pathways, and expanded families of amino acid and oligopeptide membrane transporters. The dramatic up-regulation of transcripts coding for small secreted proteins, secreted hydrolytic enzymes, and transporters in planta suggests that they play a role in host infection and nutrient acquisition. Some of these genomic hallmarks are mirrored in the genomes of other microbial eukaryotes that have independently evolved to infect plants, indicating convergent adaptation to a biotrophic existence inside plant cells.


The Plant Cell | 2010

The Chlorella variabilis NC64A Genome Reveals Adaptation to Photosymbiosis, Coevolution with Viruses, and Cryptic Sex

Guillaume Blanc; Garry A. Duncan; Irina V. Agarkova; Mark Borodovsky; James R. Gurnon; Alan Kuo; Erika Lindquist; Susan Lucas; Jasmyn Pangilinan; Juergen Polle; Asaf Salamov; Astrid Terry; Takashi Yamada; David D. Dunigan; Igor V. Grigoriev; Jean-Michel Claverie; James L. Van Etten

This report describes the genome sequence of Chlorella variabilis NC64A. Surprisingly, given that NC64A has been thought to be asexual and nonmotile, this work identifies homologs of genes involved in meiosis, gamete fusion, and flagella. Chlorella variabilis NC64A, a unicellular photosynthetic green alga (Trebouxiophyceae), is an intracellular photobiont of Paramecium bursaria and a model system for studying virus/algal interactions. We sequenced its 46-Mb nuclear genome, revealing an expansion of protein families that could have participated in adaptation to symbiosis. NC64A exhibits variations in GC content across its genome that correlate with global expression level, average intron size, and codon usage bias. Although Chlorella species have been assumed to be asexual and nonmotile, the NC64A genome encodes all the known meiosis-specific proteins and a subset of proteins found in flagella. We hypothesize that Chlorella might have retained a flagella-derived structure that could be involved in sexual reproduction. Furthermore, a survey of phytohormone pathways in chlorophyte algae identified algal orthologs of Arabidopsis thaliana genes involved in hormone biosynthesis and signaling, suggesting that these functions were established prior to the evolution of land plants. We show that the ability of Chlorella to produce chitinous cell walls likely resulted from the capture of metabolic genes by horizontal gene transfer from algal viruses, prokaryotes, or fungi. Analysis of the NC64A genome substantially advances our understanding of the green lineage evolution, including the genomic interplay with viruses and symbiosis between eukaryotes.


Proceedings of the National Academy of Sciences of the United States of America | 2011

Obligate Biotrophy Features Unraveled by the Genomic Analysis of the Rust Fungi, Melampsora larici-populina and Puccinia graminis f. sp. tritici

Sébastien Duplessis; Christina A. Cuomo; Yao-Cheng Lin; Andrea Aerts; Emilie Tisserant; Claire Veneault-Fourrey; David L. Joly; Stéphane Hacquard; Joelle Amselem; Brandi L. Cantarel; Readman Chiu; Pedro Couthinho; Nicolas Feau; Matthew A. Field; Pascal Frey; Eric Gelhaye; Jonathan M. Goldberg; Manfred Grabherr; Chinnappa D. Kodira; Annegret Kohler; Ursula Kües; Erika Lindquist; Susan Lucas; Rohit Mago; Evan Mauceli; Emmanuelle Morin; Claude Murat; Jasmyn Pangilinan; Robert F. Park; Matthew Pearson

Rust fungi are some of the most devastating pathogens of crop plants. They are obligate biotrophs, which extract nutrients only from living plant tissues and cannot grow apart from their hosts. Their lifestyle has slowed the dissection of molecular mechanisms underlying host invasion and avoidance or suppression of plant innate immunity. We sequenced the 101-Mb genome of Melampsora larici-populina, the causal agent of poplar leaf rust, and the 89-Mb genome of Puccinia graminis f. sp. tritici, the causal agent of wheat and barley stem rust. We then compared the 16,399 predicted proteins of M. larici-populina with the 17,773 predicted proteins of P. graminis f. sp tritici. Genomic features related to their obligate biotrophic lifestyle include expanded lineage-specific gene families, a large repertoire of effector-like small secreted proteins, impaired nitrogen and sulfur assimilation pathways, and expanded families of amino acid and oligopeptide membrane transporters. The dramatic up-regulation of transcripts coding for small secreted proteins, secreted hydrolytic enzymes, and transporters in planta suggests that they play a role in host infection and nutrient acquisition. Some of these genomic hallmarks are mirrored in the genomes of other microbial eukaryotes that have independently evolved to infect plants, indicating convergent adaptation to a biotrophic existence inside plant cells.


Genome Research | 2011

Comparative genomics of citric-acid-producing Aspergillus niger ATCC 1015 versus enzyme-producing CBS 513.88

Mikael Rørdam Andersen; Margarita Salazar; Peter J. Schaap; Peter J. I. van de Vondervoort; David E. Culley; Jette Thykaer; Jens Christian Frisvad; Kristian Fog Nielsen; Richard Albang; Kaj Albermann; Randy M. Berka; Gerhard H. Braus; Susanna A. Braus-Stromeyer; Luis M. Corrochano; Piet W.M. van Dijck; Gerald Hofmann; Linda L. Lasure; Jon K. Magnuson; Hildegard Menke; Martin Meijer; Susan Lisette Meijer; Jakob Blæsbjerg Nielsen; Michael Lynge Nielsen; Albert J.J. van Ooyen; Herman Jan Pel; Lars Kongsbak Poulsen; R.A. Samson; Hein Stam; Adrian Tsang; Johannes Maarten Van Den Brink

The filamentous fungus Aspergillus niger exhibits great diversity in its phenotype. It is found globally, both as marine and terrestrial strains, produces both organic acids and hydrolytic enzymes in high amounts, and some isolates exhibit pathogenicity. Although the genome of an industrial enzyme-producing A. niger strain (CBS 513.88) has already been sequenced, the versatility and diversity of this species compel additional exploration. We therefore undertook whole-genome sequencing of the acidogenic A. niger wild-type strain (ATCC 1015) and produced a genome sequence of very high quality. Only 15 gaps are present in the sequence, and half the telomeric regions have been elucidated. Moreover, sequence information from ATCC 1015 was used to improve the genome sequence of CBS 513.88. Chromosome-level comparisons uncovered several genome rearrangements, deletions, a clear case of strain-specific horizontal gene transfer, and identification of 0.8 Mb of novel sequence. Single nucleotide polymorphisms per kilobase (SNPs/kb) between the two strains were found to be exceptionally high (average: 7.8, maximum: 160 SNPs/kb). High variation within the species was confirmed with exo-metabolite profiling and phylogenetics. Detailed lists of alleles were generated, and genotypic differences were observed to accumulate in metabolic pathways essential to acid production and protein synthesis. A transcriptome analysis supported up-regulation of genes associated with biosynthesis of amino acids that are abundant in glucoamylase A, tRNA-synthases, and protein transporters in the protein producing CBS 513.88 strain. Our results and data sets from this integrative systems biology analysis resulted in a snapshot of fungal evolution and will support further optimization of cell factories based on filamentous fungi.


Proceedings of the National Academy of Sciences of the United States of America | 2011

Niche of harmful alga Aureococcus anophagefferens revealed through ecogenomics.

Christopher J. Gobler; Dianna L. Berry; Sonya T. Dyhrman; Steven W. Wilhelm; Asaf Salamov; Alexei V. Lobanov; Yan Zhang; Jackie L. Collier; Louie L. Wurch; Adam B. Kustka; Brian D. Dill; Manesh Shah; Nathan C. VerBerkmoes; Alan Kuo; Astrid Terry; Jasmyn Pangilinan; Erika Lindquist; Susan Lucas; Ian T. Paulsen; Theresa K. Hattenrath-Lehmann; Stephanie C. Talmage; Elyse A. Walker; Florian Koch; Amanda Burson; Maria Alejandra Marcoval; Ying Zhong Tang; Gary R. LeCleir; Kathryn J. Coyne; Gry Mine Berg; Erin M. Bertrand

Harmful algal blooms (HABs) cause significant economic and ecological damage worldwide. Despite considerable efforts, a comprehensive understanding of the factors that promote these blooms has been lacking, because the biochemical pathways that facilitate their dominance relative to other phytoplankton within specific environments have not been identified. Here, biogeochemical measurements showed that the harmful alga Aureococcus anophagefferens outcompeted co-occurring phytoplankton in estuaries with elevated levels of dissolved organic matter and turbidity and low levels of dissolved inorganic nitrogen. We subsequently sequenced the genome of A. anophagefferens and compared its gene complement with those of six competing phytoplankton species identified through metaproteomics. Using an ecogenomic approach, we specifically focused on gene sets that may facilitate dominance within the environmental conditions present during blooms. A. anophagefferens possesses a larger genome (56 Mbp) and has more genes involved in light harvesting, organic carbon and nitrogen use, and encoding selenium- and metal-requiring enzymes than competing phytoplankton. Genes for the synthesis of microbial deterrents likely permit the proliferation of this species, with reduced mortality losses during blooms. Collectively, these findings suggest that anthropogenic activities resulting in elevated levels of turbidity, organic matter, and metals have opened a niche within coastal ecosystems that ideally suits the unique genetic capacity of A. anophagefferens and thus, has facilitated the proliferation of this and potentially other HABs.


Genome Biology | 2012

The genome of the polar eukaryotic microalga Coccomyxa subellipsoidea reveals traits of cold adaptation

Guillaume Blanc; Irina V. Agarkova; Jane Grimwood; Alan Kuo; Andrew J. Brueggeman; David D. Dunigan; James R. Gurnon; Istvan Ladunga; Erika Lindquist; Susan Lucas; Jasmyn Pangilinan; Thomas Pröschold; Asaf Salamov; Jeremy Schmutz; Donald P. Weeks; Takashi Yamada; Alexandre Lomsadze; Mark Borodovsky; Jean-Michel Claverie; Igor V. Grigoriev; James L. Van Etten

BackgroundLittle is known about the mechanisms of adaptation of life to the extreme environmental conditions encountered in polar regions. Here we present the genome sequence of a unicellular green alga from the division chlorophyta, Coccomyxa subellipsoidea C-169, which we will hereafter refer to as C-169. This is the first eukaryotic microorganism from a polar environment to have its genome sequenced.ResultsThe 48.8 Mb genome contained in 20 chromosomes exhibits significant synteny conservation with the chromosomes of its relatives Chlorella variabilis and Chlamydomonas reinhardtii. The order of the genes is highly reshuffled within synteny blocks, suggesting that intra-chromosomal rearrangements were more prevalent than inter-chromosomal rearrangements. Remarkably, Zepp retrotransposons occur in clusters of nested elements with strictly one cluster per chromosome probably residing at the centromere. Several protein families overrepresented in C. subellipsoidae include proteins involved in lipid metabolism, transporters, cellulose synthases and short alcohol dehydrogenases. Conversely, C-169 lacks proteins that exist in all other sequenced chlorophytes, including components of the glycosyl phosphatidyl inositol anchoring system, pyruvate phosphate dikinase and the photosystem 1 reaction center subunit N (PsaN).ConclusionsWe suggest that some of these gene losses and gains could have contributed to adaptation to low temperatures. Comparison of these genomic features with the adaptive strategies of psychrophilic microbes suggests that prokaryotes and eukaryotes followed comparable evolutionary routes to adapt to cold environments.

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Erika Lindquist

United States Department of Energy

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Asaf Salamov

Baylor College of Medicine

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Harris Shapiro

United States Department of Energy

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Igor V. Grigoriev

United States Department of Energy

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Susan Lucas

Joint Genome Institute

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Alan Kuo

United States Department of Energy

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Andrea Aerts

United States Department of Energy

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Kerrie Barry

United States Department of Energy

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Anna Lipzen

United States Department of Energy

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