Gwênlyn Glusman

Dr. Gwênlyn Glusman

Institute for Systems Biology, Seattle, WA 98109, USA
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orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 August 2002 in Science
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Journal Article
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SASamuel Aparicio
Samuel Aparicio
JCJarrod Chapman
Jarrod Chapman
ESElia Stupka
Elia Stupka
NPNik Putnam
Nik Putnam
JCJer-Ming Chia
Jer-Ming Chia
SBSydney Brenner
Sydney Brenner
The compact genome of Fugu rubripes has been sequenced to over 95% coverage, and more than 80% of the assembly is in multigene-sized scaffolds. In this 365-megabase vertebrate genome, repetitive DNA accounts for less than one-sixth of the sequence, and gene loci occupy about one-third of the genome. As with the human genome, gene loci are not evenly distributed, but are clustered into sparse and dense regions. Some “giant” genes were observed that had average coding sequence sizes but were spread over genomic lengths significantly larger than those of their human orthologs. Although three-quarters of predicted human proteins have a strong match to Fugu , approximately a quarter of the human proteins had highly diverged from or had no pufferfish homologs, highlighting the extent of protein evolution in the 450 million years since teleosts and mammals diverged. Conserved linkages between Fugu and human genes indicate the preservation of chromosomal segments from the common vertebrate ancestor, but with considerable scrambling of gene order.

23 June 2005 in Proceedings of the National Academy of Sciences
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Journal Article
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Jared C RoachJared C Roach
Jared C Roach
GGGwênlyn Glusman
Gwênlyn Glusman
LRLee Rowen
Lee Rowen
AKAmardeep Kaur
Amardeep Kaur
MPMaureen Purcell
Maureen Purcell
AAAlan Aderem
Alan Aderem
The complete sequences of Takifugu Toll-like receptor (TLR) loci and gene predictions from many draft genomes enable comprehensive molecular phylogenetic analysis. Strong selective pressure for recognition of and response to pathogen-associated molecular patterns has maintained a largely unchanging TLR recognition in all vertebrates. There are six major families of vertebrate TLRs. This repertoire is distinct from that of invertebrates. TLRs within a family recognize a general class of pathogen-associated molecular patterns. Most vertebrates have exactly one gene ortholog for each TLR family. The family including TLR1 has more species-specific adaptations than other families. A major family including TLR11 is represented in humans only by a pseudogene. Coincidental evolution plays a minor role in TLR evolution. The sequencing phase of this study produced finished genomic sequences for the 12 Takifugu rubripes TLRs. In addition, we have produced >70 gene models, including sequences from the opossum, chicken, frog, dog, sea urchin, and sea squirt.

30 April 2010 in Science
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JRJared C. Roach
Jared C. Roach
GGGwênlyn Glusman
Gwênlyn Glusman
ASArian F. A. Smit
Arian F. A. Smit
CHChad D. Huff
Chad D. Huff
RHRobert Hubley
Robert Hubley
DGDavid J. Galas
David J. Galas
Runs in the Family: The power to detect mutations involved in disease by genome sequencing is enhanced when combined with the ability to discover specific mutations that may have arisen between offspring and parents. Roach et al. (p. 636 , published online 10 March) present the sequence of a family with two offspring affected with two genetic disorders: Miller syndrome and primary ciliary dyskinesia. Sequence analysis of the children and their parents not only showed that the intergenerational mutation rate was lower than anticipated but also revealed recombination sites and the occurrence of rare polymorphisms.

18 February 2021 in Nature Metabolism
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TWTomasz Wilmanski
Tomasz Wilmanski
CDChristian Diener
Christian Diener
NRNoa Rappaport
Noa Rappaport
SPSushmita Patwardhan
Sushmita Patwardhan
JWJack Wiedrick
Jack Wiedrick
NPNathan Price
Nathan Price

1 May 2001 in Genome Research
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Journal Article
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GGGwênlyn Glusman
Gwênlyn Glusman
IYItai Yanai
Itai Yanai
IRIrit Rubin
Irit Rubin
DLDoron Lancet
Doron Lancet
Olfactory receptors likely constitute the largest gene superfamily in the vertebrate genome. Here we present the nearly complete human olfactory subgenome elucidated by mining the genome draft with gene discovery algorithms. Over 900 olfactory receptor genes and pseudogenes (ORs) were identified, two-thirds of which were not annotated previously. The number of extrapolated ORs is in good agreement with previous theoretical predictions. The sequence of at least 63% of the ORs is disrupted by what appears to be a random process of pseudogene formation. ORs constitute 17 gene families, 4 of which contain more than 100 members each. “Fish-like” Class I ORs, previously considered a relic in higher tetrapods, constitute as much as 10% of the human repertoire, all in one large cluster on chromosome 11. Their lower pseudogene fraction suggests a functional significance. ORs are disposed on all human chromosomes except 20 and Y, and nearly 80% are found in clusters of 6–138 genes. A novel comparative cluster analysis was used to trace the evolutionary path that may have led to OR proliferation and diversification throughout the genome. The results of this analysis suggest the following genome expansion history: first, the generation of a “tetrapod-specific” Class II OR cluster on chromosome 11 by local duplication, then a single-step duplication of this cluster to chromosome 1, and finally an avalanche of duplication events out of chromosome 1 to most other chromosomes. The results of the data mining and characterization of ORs can be accessed at the Human Olfactory Receptor Data Exploratorium Web site (http://bioinfo.weizmann.ac.il/HORDE).

5 August 2013 in Personalized Medicine
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Journal Article
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MFMauricio Flores
Mauricio Flores
GGGwênlyn Glusman
Gwênlyn Glusman
KBKristin Brogaard
Kristin Brogaard
NPNathan Price
Nathan Price
LHLeroy Hood
Leroy Hood
Ten years ago, the proposition that healthcare is evolving from reactive disease care to care that is predictive, preventive, personalized and participatory was regarded as highly speculative. Today, the core elements of that vision are widely accepted and have been articulated in a series of recent reports by the US Institute of Medicine. Systems approaches to biology and medicine are now beginning to provide patients, consumers and physicians with personalized information about each individual’s unique health experience of both health and disease at the molecular, cellular and organ levels. This information will make disease care radically more cost effective by personalizing care to each person’s unique biology and by treating the causes rather than the symptoms of disease. It will also provide the basis for concrete action by consumers to improve their health as they observe the impact of lifestyle decisions. Working together in digitally powered familial and affinity networks, consumers will be able ...