Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Jimmy H. Saw is active.

Publication


Featured researches published by Jimmy H. Saw.


Nature | 2008

The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus)

Ray Ming; Shaobin Hou; Yun Feng; Qingyi Yu; Alexandre Dionne-Laporte; Jimmy H. Saw; Pavel Senin; Wei Wang; Benjamin V. Ly; Kanako L. T. Lewis; Lu Feng; Meghan R. Jones; Rachel L. Skelton; Jan E. Murray; Cuixia Chen; Wubin Qian; Junguo Shen; Peng Du; Moriah Eustice; Eric J. Tong; Haibao Tang; Eric Lyons; Robert E. Paull; Todd P. Michael; Kerr Wall; Danny W. Rice; Henrik H. Albert; Ming Li Wang; Yun J. Zhu; Michael C. Schatz

Papaya, a fruit crop cultivated in tropical and subtropical regions, is known for its nutritional benefits and medicinal applications. Here we report a 3× draft genome sequence of ‘SunUp’ papaya, the first commercial virus-resistant transgenic fruit tree to be sequenced. The papaya genome is three times the size of the Arabidopsis genome, but contains fewer genes, including significantly fewer disease-resistance gene analogues. Comparison of the five sequenced genomes suggests a minimal angiosperm gene set of 13,311. A lack of recent genome duplication, atypical of other angiosperm genomes sequenced so far, may account for the smaller papaya gene number in most functional groups. Nonetheless, striking amplifications in gene number within particular functional groups suggest roles in the evolution of tree-like habit, deposition and remobilization of starch reserves, attraction of seed dispersal agents, and adaptation to tropical daylengths. Transgenesis at three locations is closely associated with chloroplast insertions into the nuclear genome, and with topoisomerase I recognition sites. Papaya offers numerous advantages as a system for fruit-tree functional genomics, and this draft genome sequence provides the foundation for revealing the basis of Carica’s distinguishing morpho-physiological, medicinal and nutritional properties.


Nature | 2007

Methane oxidation by an extremely acidophilic bacterium of the phylum Verrucomicrobia

Peter F. Dunfield; Anton Yuryev; Pavel Senin; Angela V. Smirnova; Matthew B. Stott; Shaobin Hou; Binh Ly; Jimmy H. Saw; Zhemin Zhou; Yan Ren; Jianmei Wang; Bruce W. Mountain; Michelle A. Crowe; Tina M. Weatherby; Paul L. E. Bodelier; Werner Liesack; Lu Feng; Lei Wang; Maqsudul Alam

Aerobic methanotrophic bacteria consume methane as it diffuses away from methanogenic zones of soil and sediment. They act as a biofilter to reduce methane emissions to the atmosphere, and they are therefore targets in strategies to combat global climate change. No cultured methanotroph grows optimally below pH 5, but some environments with active methane cycles are very acidic. Here we describe an extremely acidophilic methanotroph that grows optimally at pH 2.0–2.5. Unlike the known methanotrophs, it does not belong to the phylum Proteobacteria but rather to the Verrucomicrobia, a widespread and diverse bacterial phylum that primarily comprises uncultivated species with unknown genotypes. Analysis of its draft genome detected genes encoding particulate methane monooxygenase that were homologous to genes found in methanotrophic proteobacteria. However, known genetic modules for methanol and formaldehyde oxidation were incomplete or missing, suggesting that the bacterium uses some novel methylotrophic pathways. Phylogenetic analysis of its three pmoA genes (encoding a subunit of particulate methane monooxygenase) placed them into a distinct cluster from proteobacterial homologues. This indicates an ancient divergence of Verrucomicrobia and Proteobacteria methanotrophs rather than a recent horizontal gene transfer of methanotrophic ability. The findings show that methanotrophy in the Bacteria is more taxonomically, ecologically and genetically diverse than previously thought, and that previous studies have failed to assess the full diversity of methanotrophs in acidic environments.


Nature | 2017

Asgard archaea illuminate the origin of eukaryotic cellular complexity

Katarzyna Zaremba-Niedzwiedzka; Eva F. Caceres; Jimmy H. Saw; Disa Bäckström; Lina Juzokaite; Emmelien Vancaester; Kiley W. Seitz; Karthik Anantharaman; Piotr Starnawski; Kasper Urup Kjeldsen; Matthew B. Stott; Takuro Nunoura; Jillian F. Banfield; Andreas Schramm; Brett J. Baker; Anja Spang; Thijs J. G. Ettema

The origin and cellular complexity of eukaryotes represent a major enigma in biology. Current data support scenarios in which an archaeal host cell and an alphaproteobacterial (mitochondrial) endosymbiont merged together, resulting in the first eukaryotic cell. The host cell is related to Lokiarchaeota, an archaeal phylum with many eukaryotic features. The emergence of the structural complexity that characterizes eukaryotic cells remains unclear. Here we describe the ‘Asgard’ superphylum, a group of uncultivated archaea that, as well as Lokiarchaeota, includes Thor-, Odin- and Heimdallarchaeota. Asgard archaea affiliate with eukaryotes in phylogenomic analyses, and their genomes are enriched for proteins formerly considered specific to eukaryotes. Notably, thorarchaeal genomes encode several homologues of eukaryotic membrane-trafficking machinery components, including Sec23/24 and TRAPP domains. Furthermore, we identify thorarchaeal proteins with similar features to eukaryotic coat proteins involved in vesicle biogenesis. Our results expand the known repertoire of ‘eukaryote-specific’ proteins in Archaea, indicating that the archaeal host cell already contained many key components that govern eukaryotic cellular complexity.


Proceedings of the National Academy of Sciences of the United States of America | 2004

Genome sequence of the deep-sea γ-proteobacterium Idiomarina loihiensis reveals amino acid fermentation as a source of carbon and energy

Shaobin Hou; Jimmy H. Saw; Kit Shan Lee; Tracey Freitas; Claude Belisle; Yutaka Kawarabayasi; Stuart P. Donachie; Alla Pikina; Michael Y. Galperin; Eugene V. Koonin; Kira S. Makarova; Marina V. Omelchenko; Alexander V. Sorokin; Yuri I. Wolf; Qing X. Li; Young Soo Keum; Sonia Campbell; Judith R. Denery; Shinichi Aizawa; Satoshi Shibata; Alexander Malahoff; Maqsudul Alam

We report the complete genome sequence of the deep-sea γ-proteobacterium, Idiomarina loihiensis, isolated recently from a hydrothermal vent at 1,300-m depth on the Lōihi submarine volcano, Hawaii. The I. loihiensis genome comprises a single chromosome of 2,839,318 base pairs, encoding 2,640 proteins, four rRNA operons, and 56 tRNA genes. A comparison of I. loihiensis to the genomes of other γ-proteobacteria reveals abundance of amino acid transport and degradation enzymes, but a loss of sugar transport systems and certain enzymes of sugar metabolism. This finding suggests that I. loihiensis relies primarily on amino acid catabolism, rather than on sugar fermentation, for carbon and energy. Enzymes for biosynthesis of purines, pyrimidines, the majority of amino acids, and coenzymes are encoded in the genome, but biosynthetic pathways for Leu, Ile, Val, Thr, and Met are incomplete. Auxotrophy for Val and Thr was confirmed by in vivo experiments. The I. loihiensis genome contains a cluster of 32 genes encoding enzymes for exopolysaccharide and capsular polysaccharide synthesis. It also encodes diverse peptidases, a variety of peptide and amino acid uptake systems, and versatile signal transduction machinery. We propose that the source of amino acids for I. loihiensis growth are the proteinaceous particles present in the deep sea hydrothermal vent waters. I. loihiensis would colonize these particles by using the secreted exopolysaccharide, digest these proteins, and metabolize the resulting peptides and amino acids. In summary, the I. loihiensis genome reveals an integrated mechanism of metabolic adaptation to the constantly changing deep-sea hydrothermal ecosystem.


Genetics | 2007

Construction of a Sequence-Tagged High-Density Genetic Map of Papaya for Comparative Structural and Evolutionary Genomics in Brassicales

Cuixia Chen; Qingyi Yu; Shaobin Hou; Ying jun Li; Moriah Eustice; Rachel L. Skelton; Olivia Veatch; Rachel E. Herdes; Lauren Diebold; Jimmy H. Saw; Yun Feng; Wubin Qian; Lee H. Bynum; Lei Wang; Paul H. Moore; Robert E. Paull; Maqsudul Alam; Ray Ming

A high-density genetic map of papaya (Carica papaya L.) was constructed using microsatellite markers derived from BAC end sequences and whole-genome shot gun sequences. Fifty-four F2 plants derived from varieties AU9 and SunUp were used for linkage mapping. A total of 707 markers, including 706 microsatellite loci and the morphological marker fruit flesh color, were mapped into nine major and three minor linkage groups. The resulting map spanned 1069.9 cM with an average distance of 1.5 cM between adjacent markers. This sequence-based microsatellite map resolved the very large linkage group 2 (LG 2) of the previous high-density map using amplified fragment length polymorphism markers. The nine major LGs of our map represent papayas haploid nine chromosomes with LG 1 of the sex chromosome being the largest. This map validates the suppression of recombination at the male-specific region of the Y chromosome (MSY) mapped on LG 1 and at potential centromeric regions of other LGs. Segregation distortion was detected in a large region on LG 1 surrounding the MSY region due to the abortion of the YY genotype and in a region of LG6 due to an unknown cause. This high-density sequence-tagged genetic map is being used to integrate genetic and physical maps and to assign genome sequence scaffolds to papaya chromosomes. It provides a framework for comparative structural and evolutional genomic research in the order Brassicales.


Archaea | 2013

Close Encounters of the Third Domain : The Emerging Genomic View of Archaeal Diversity and Evolution

Anja Spang; Joran Martijn; Jimmy H. Saw; Anders E. Lind; Lionel Guy; Thijs J. G. Ettema

The Archaea represent the so-called Third Domain of life, which has evolved in parallel with the Bacteria and which is implicated to have played a pivotal role in the emergence of the eukaryotic domain of life. Recent progress in genomic sequencing technologies and cultivation-independent methods has started to unearth a plethora of data of novel, uncultivated archaeal lineages. Here, we review how the availability of such genomic data has revealed several important insights into the diversity, ecological relevance, metabolic capacity, and the origin and evolution of the archaeal domain of life.


Standards in Genomic Sciences | 2012

Complete genome sequencing and analysis of Saprospira grandis str. Lewin, a predatory marine bacterium

Jimmy H. Saw; Anton Yuryev; Masaomi Kanbe; Shaobin Hou; Aaron G. Young; Shin-Ichi Aizawa; Maqsudul Alam

Saprospira grandis is a coastal marine bacterium that can capture and prey upon other marine bacteria using a mechanism known as ‘ixotrophy’. Here, we present the complete genome sequence of Saprospira grandis str. Lewin isolated from La Jolla beach in San Diego, California. The complete genome sequence comprises a chromosome of 4.35 Mbp and a plasmid of 54.9 Kbp. Genome analysis revealed incomplete pathways for the biosynthesis of nine essential amino acids but presence of a large number of peptidases. The genome encodes multiple copies of sensor globin-coupled rsbR genes thought to be essential for stress response and the presence of such sensor globins in Bacteroidetes is unprecedented. A total of 429 spacer sequences within the three CRISPR repeat regions were identified in the genome and this number is the largest among all the Bacteroidetes sequenced to date.


The ISME Journal | 2014

'Geoarchaeote NAG1' is a deeply rooting lineage of the archaeal order Thermoproteales rather than a new phylum

Lionel Guy; Anja Spang; Jimmy H. Saw; Thijs J. G. Ettema

‘Geoarchaeote NAG1’ is a deeply rooting lineage of the archaeal order Thermoproteales rather than a new phylum


PLOS Genetics | 2018

Asgard archaea are the closest prokaryotic relatives of eukaryotes

Anja Spang; Laura Eme; Jimmy H. Saw; Eva F. Caceres; Katarzyna Zaremba-Niedzwiedzka; Jonathan Lombard; Lionel Guy; Thijs J. G. Ettema

In Spang et al. [1], we reported the discovery of Lokiarchaeum (Loki1) and two related lineages (Loki2 and Loki3, now referred to as Heimdallarchaeote LC_2 and LC_3). These were the first known representatives of the subsequently described Asgard superphylum [2], which branches as a sister clade to the TACK archaea [3]. We provided extensive phylogenomic evidence for the emergence of eukaryotes from within the Asgard archaea (thus supporting the two-domains [2D] tree of life), and the investigation of the Lokiarchaeum genome revealed the presence of more eukaryotic signature proteins (ESPs) than in any other described archaeal lineage [1]. In the recent study by Da Cunha et al. [4], the authors argue against the findings reported in Spang et al. Their main claims are that (i) the published genome data contains extensive contamination from distantly related organisms; (ii) a subset of universal genes supports a three-domains (3D) tree of life; and (iii) removing the elongation factor 2 (EF2) from the phylogenomic analysis breaks the Lokiarchaeota–Eukarya affiliation. Below, we show that the claims by Da Cunha et al. are unfounded.


Nature | 2015

Complex archaea that bridge the gap between prokaryotes and eukaryotes

Anja Spang; Jimmy H. Saw; Steffen Leth Jørgensen; Katarzyna Zaremba-Niedzwiedzka; Joran Martijn; Anders E. Lind; Roel van Eijk; Christa Schleper; Lionel Guy; Thijs J. G. Ettema

Collaboration


Dive into the Jimmy H. Saw's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Qingyi Yu

Fujian Agriculture and Forestry University

View shared research outputs
Top Co-Authors

Avatar

Paul H. Moore

Agricultural Research Service

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Pavel Senin

Los Alamos National Laboratory

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge