Vivek Kumar

Vivek Kumar
  • PhD
  • Professor (Assistant) at The Jackson Laboratory

About

109
Publications
20,926
Reads
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5,348
Citations
Current institution
The Jackson Laboratory
Current position
  • Professor (Assistant)
Additional affiliations
June 1995 - August 1997
University of Chicago
Position
  • Research Assistant
February 2009 - December 2014
University of Texas Southwestern Medical Center
Position
  • Instructor
January 2004 - January 2009
Northwestern University
Position
  • PostDoc Position

Publications

Publications (109)
Article
Frailty indexes (FIs) capture health status in humans and model organisms. To accelerate our understanding of biological aging and carry out scalable interventional studies, high-throughput approaches are necessary. We previously introduced a machine vision-based visual frailty index (vFI) that uses mouse behavior in the open field to assess frailt...
Preprint
Full-text available
Frailty indexes (FIs) capture health status in humans and model organisms. To accelerate our understanding of biological aging and carry out scalable interventional studies, high-throughput approaches are necessary. We previously introduced a machine vision-based visual frailty index (vFI) that uses mouse behavior in the open field to assess frailt...
Article
Full-text available
Changes in body mass are key indicators of health in humans and animals and are routinely monitored in animal husbandry and preclinical studies. In rodent studies, the current method of manually weighing the animal on a balance causes at least two issues. First, directly handling the animal induces stress, possibly confounding studies. Second, thes...
Preprint
Full-text available
Seizures are caused by abnormally synchronous brain activity that can result in changes in muscle tone, such as twitching, stiffness, limpness, or rhythmic jerking. These behavioral manifestations are clear on visual inspection and the most widely used seizure scoring systems in preclinical models, such as the Racine scale in rodents, use these beh...
Article
Full-text available
Drugs of abuse induce neuroadaptations, including synaptic plasticity, that are critical for transition to addiction, and genes and pathways that regulate these neuroadaptations are potential therapeutic targets. Tropomodulin 2 (Tmod2) is an actin-regulating gene that plays an important role in synapse maturation and dendritic arborization and has...
Article
Full-text available
Substance use disorders are heritable disorders characterized by compulsive drug use, the biological mechanisms for which remain largely unknown. Genetic correlations reveal that predisposing drug‐naïve phenotypes, including anxiety, depression, novelty preference and sensation seeking, are predictive of drug‐use phenotypes, thereby implicating sha...
Preprint
1 Summary Changes in body mass are a key indicator of health and disease in humans and model organisms. Animal body mass is routinely monitored in husbandry and preclinical studies. In rodent studies, the current best method requires manually weighing the animal on a balance which has at least two consequences. First, direct handling of the animal...
Article
Full-text available
Background Since the origin of the C57BL/6 (B6) mouse strain, several phenotypically and genetically distinct B6 substrains have emerged. For example, C57BL/6J mice (B6J) display greater voluntary ethanol consumption and locomotor response to psychostimulants and differences in nucleus accumbens synaptic physiology relative to C57BL/6N (B6N) mice....
Preprint
Full-text available
Substance use disorders (SUDs) are heritable disorders characterized by compulsive drug use, but the biological mechanisms driving addiction remain largely unknown. Genetic correlations reveal that predisposing drug-naive phenotypes, including anxiety, depression, novelty preference, and sensation seeking, are predictive of drug-use phenotypes, imp...
Article
Full-text available
The mammalian circadian system generates an approximate 24-h rhythm through a complex autoregulatory feedback loop. Four genes, Period1 (Per1), Period2 (Per2), Cryptochrome1 (Cry1), and Cryptochrome2 (Cry2), regulate the negative feedback within this loop. Although these proteins have distinct roles within the core circadian mechanism, their indivi...
Article
Full-text available
Although a wide variety of genetic tools has been developed to study learning and memory, the molecular basis of memory encoding remains incompletely understood. Here, we undertook an unbiased approach to identify novel genes critical for memory encoding. From a large-scale, in vivo mutagenesis screen using contextual fear conditioning, we isolated...
Article
Full-text available
Heterogeneity in biological aging manifests itself in health status and mortality. Frailty indices (FIs) capture health status in humans and model organisms. To accelerate our understanding of biological aging and carry out scalable interventional studies, high-throughput approaches are necessary. Here we introduce a machine-learning-based visual F...
Preprint
Real-world behavior is often shaped by complex interactions between multiple agents. To scalably study multi-agent behavior, advances in unsupervised and self-supervised learning have enabled a variety of different behavioral representations to be learned from trajectory data. To date, there does not exist a unified set of benchmarks that can enabl...
Article
Real-world behavior is often shaped by complex interactions between multiple agents. To scalably study multi-agent behavior, advances in unsupervised and self-supervised learning have enabled a variety of different behavioral representations to be learned from trajectory data. To date, there does not exist a unified set of benchmarks that can enabl...
Preprint
Automated detection of complex animal behavior remains a challenge in behavioral neurogenetics. Developments in computer-vision have greatly advanced automated behavior detection and allow high-throughput pre-clinical studies. An integrated hardware and software solution is necessary to facilitate the adoption of these advances in the field of beha...
Article
Full-text available
Gait and posture are often perturbed in many neurological, neuromuscular, and neuropsychiatric conditions. Rodents provide a tractable model for elucidating disease mechanisms and interventions. Here, we develop a neural-network-based assay that adopts the commonly used open field apparatus for mouse gait and posture analysis. We quantitate both wi...
Article
Full-text available
Forward genetics is a powerful approach based on chromosomal mapping of phenotypes and has successfully led to the discovery of many mouse mutations in genes responsible for various phenotypes. Although crossing between genetically remote strains can produce F2 and backcross mice for chromosomal mapping, the phenotypes are often affected by backgro...
Article
Study Objectives Sleep is an important biological process that is perturbed in numerous diseases, and assessment its substages currently requires implantation of electrodes to carry out electroencephalogram/electromyogram (EEG/EMG) analysis. Although accurate, this method comes at a high cost of invasive surgery and experts trained to score EEG/EMG...
Preprint
Full-text available
Chronological aging is uniform, but biological aging is heterogeneous. Clinically, this heterogeneity manifests itself in health status and mortality, and it distinguishes healthy from unhealthy aging. Clinical frailty indexes (FIs) serve as an important tool in gerontology to capture health status. FIs have been adapted for use in mice and are an...
Article
Full-text available
Identifying the genetic determinants of pain is a scientific imperative given the magnitude of the global health burden that pain causes. Here, we report a genetic screen for nociception, performed under the auspices of the International Mouse Phenotyping Consortium. A biased set of 110 single-gene knockout mouse strains was screened for 1 or more...
Article
Full-text available
ELife digest Behavior is one of the ultimate and most complex outputs of the body’s central nervous system, which controls movement, emotion and mood. It is also influenced by a person’s genetics. Scientists studying the link between behavior and genetics often conduct experiments using animals, whose actions can be more easily characterized than h...
Preprint
Full-text available
Gait and whole body posture are sensitive measures of the proper functioning of numerous neural circuits, and are often perturbed in many neurological, neuromuscular, and neuropsychiatric illnesses. Rodents provide a tractable model for elucidating disease mechanisms and interventions, however, studying gait and whole body posture in rodent models...
Article
The laboratory mouse is the most widely used animal model for biomedical research, due in part to its well annotated genome, wealth of genetic resources and the ability to precisely manipulate its genome. Despite the importance of genetics for mouse research, genetic quality control (QC) is not standardized, in part due to the lack of cost effectiv...
Preprint
Full-text available
Automated detection of complex animal behaviors remains a challenging problem in neuroscience, particularly for behaviors that consist of disparate sequential motions. Grooming, a prototypical stereotyped behavior, is often used as an endophenotype in psychiatric genetics. Using mouse grooming behavior as an example, we develop a general purpose ne...
Article
Full-text available
The discovery and development of new and potentially nonaddictive pain therapeutics requires rapid, yet clinically relevant assays of nociception in preclinical models. A reliable and scalable automated scoring system for nocifensive behavior of mice in the formalin assay would dramatically lower the time and labor costs associated with experiments...
Article
Full-text available
Background In alcohol‐dependent individuals, acute alcohol withdrawal results in severe physiological disruption, including potentially lethal central nervous system hyperexcitability. Although benzodiazepines successfully mitigate such symptoms, this treatment does not significantly reduce recidivism rates in postdependent individuals. Instead, pe...
Preprint
Full-text available
The laboratory mouse is the most widely used animal model for biomedical research, due in part to its well annotated genome, wealth of genetic resources and the ability to precisely manipulate its genome. Despite the importance of genetics for mouse research, genetic quality control (QC) is not standardized, in part due to the lack of cost effectiv...
Article
Full-text available
Fumarylacetoacetate hydrolase (FAH) is the last enzyme in tyrosine catabolism, and mutations in the FAH gene are associated with hereditary tyrosinemia type I (HT1 or TYRSN1) in humans. In a behavioral screen of N -ethyl- N -nitrosourea mutagenized mice we identified a mutant line which we named “ swingshift ” ( swst , MGI:3611216) with a nonsynony...
Article
Full-text available
Motivation: High-throughput phenomic projects generate complex data from small treatment and large control groups that increase the power of the analyses but introduce variation over time. A method is needed to utlize a set of temporally local controls that maximises analytic power while minimising noise from unspecified environmental factors. Re...
Article
Full-text available
Tobacco smoking is the major cause of disability and death in the United States and around the world. In addition, tobacco dependence and addiction express themselves as complex behaviors involving an interplay of genetics, environment, and psychological state. Mouse genetic studies could potentially elucidate the novel genes and/or gene networks r...
Article
Full-text available
Binge eating (BE) is a heritable trait associated with eating disorders and involves episodes of rapid, large amounts of food consumption. We previously identified cytoplasmic FMR1-interacting protein 2 (Cyfip2) as a genetic factor underlying compulsive-like BE in mice. CYFIP2 is a homolog of CYFIP1 which is one of four paternally-deleted genes in...
Preprint
Motivation High-throughput phenomic projects generate complex data from small treatment and large control groups that increase the power of the analyses but introduce variation over time. A method is needed to utlize a set of temporally local controls that maximises analytic power while minimising noise from unspecified environmental factors. Resu...
Preprint
Full-text available
Drugs of abuse induce neuroadaptations, including synaptic plasticity, that are critical for transition to addiction, and genes and pathways that regulate these neuroadaptations are potential therapeutic targets. Tropomodulin 2 ( Tmod2 ) is an actin-regulating gene that plays an important role in synapse maturation and dendritic arborization and ha...
Article
Chronic fatigue is a debilitating disorder with widespread consequences, but effective treatment strategies are lacking. Novel genetic mouse models of fatigue may prove invaluable for studying its underlying physiological mechanisms and for testing treatments and interventions. In a screen of voluntary wheel‐running behavior in N‐ethyl‐N‐nitrosoure...
Article
Full-text available
The ability to track animals accurately is critical for behavioral experiments. For video-based assays, this is often accomplished by manipulating environmental conditions to increase contrast between the animal and the background in order to achieve proper foreground/background detection (segmentation). Modifying environmental conditions for exper...
Article
Full-text available
[This corrects the article DOI: 10.1038/s42003-018-0226-0.]. Despite advances in next generation sequencing technologies, determining the genetic basis of ocular disease remains a major challenge due to the limited access and prohibitive cost of human forward genetics. Thus, less than 4,000 genes currently have available phenotype information for a...
Article
Full-text available
Transgenesis has been a mainstay of mouse genetics for over 30 yr, providing numerous models of human disease and critical genetic tools in widespread use today. Generated through the random integration of DNA fragments into the host genome, transgenesis can lead to insertional mutagenesis if a coding gene or an essential element is disrupted, and...
Preprint
Full-text available
Sleep is a critical process that is well-conserved across mammalian species, and perhaps most animals, yet its functions and underlying mechanisms remain poorly understood. Identification of genes and pathways that can influence sleep may shed new light on these functions. Genomic screens enable the detection of previously unsuspected molecular pro...
Article
Full-text available
Despite advances in next generation sequencing technologies, determining the genetic basis of ocular disease remains a major challenge due to the limited access and prohibitive cost of human forward genetics. Thus, less than 4,000 genes currently have available phenotype information for any organ system. Here we report the ophthalmic findings from...
Article
Full-text available
We illustrate, through two case studies, that “mean-variance QTL mapping”—QTL mapping that models effects on the mean and the variance simultaneously—can discover QTL that traditional interval mapping cannot. Mean-variance QTL mapping is based on the double generalized linear model, which extends the standard linear model used in interval mapping b...
Preprint
Full-text available
The ability to track animals accurately is critical for behavioral experiments. For video-based assays, this is often accomplished by manipulating environmental conditions to increase contrast between the animal and the background, in order to achieve proper foreground/background detection (segmentation). However, as behavioral paradigms become mor...
Preprint
Full-text available
We illustrate, through two case studies, that “mean-variance QTL mapping” can discover QTL that traditional interval mapping cannot. Mean-variance QTL mapping is based on the double generalized linear model, which elaborates on the standard linear model by incorporating not only a linear model for the data itself, but also a linear model for the re...
Preprint
Full-text available
Binge eating (BE) is a heritable trait associated with eating disorders and involves consumption of a large quantity of food in a short time. We identified cytoplasmic FMRP-interacting protein 2 (Cyfip2) as a major genetic factor underlying BE and concomitant compulsive-like behaviors in mice. CYFIP2 is a gene homolog of CYFIP1-one of four paternal...
Chapter
Nearly isogenic substrains provide a simplified system for identification and validation of functional variants and the individual contributions of genes to complex traits. A reduced complexity cross (RCC) is generated by mating closely related substrains followed by crossing of the resulting F1 progeny to generate a recombinant F2 population. The...
Preprint
Full-text available
Transgenesis has been a mainstay of mouse genetics for over 30 years, providing numerous models of human disease and critical genetic tools in widespread use today. Generated through the random integration of DNA fragments into the host genome, transgenesis can lead to insertional mutagenesis if a coding gene or essential element is disrupted, and...
Preprint
In a screen of voluntary wheel-running behavior designed to identify genetic mouse models of chronic fatigue in ENU mutagenized C57BL/6J mice, we discovered two lines that showed aberrant wheel-running patterns. These lines both stem from a single original founder identified as a low body-weight candidate in a recessive screen. Progeny from both of...
Article
Full-text available
The epidermis is a highly regenerative barrier protecting organisms from environmental insults, including UV radiation, the main cause of skin cancer and skin aging. Here, we show that time-restricted feeding (RF) shifts the phase and alters the amplitude of the skin circadian clock and affects the expression of approximately 10% of the skin transc...
Article
Full-text available
Sleep is conserved from invertebrates to vertebrates, and is tightly regulated in a homeostatic manner. The molecular and cellular mechanisms that determine the amount of rapid eye movement sleep (REMS) and non-REMS (NREMS) remain unknown. Here we identify two dominant mutations that affect sleep and wakefulness by using an electroencephalogram/ele...
Article
Full-text available
The discovery of leptin substantiated the usefulness of a forward genetic approach in elucidating the molecular network regulating energy metabolism. However, no successful dominant screening for obesity has been reported, which may be due to the influence of quantitative trait loci between the screening and counter strains and the low fertility of...
Article
Full-text available
Historically, work on peripheral circadian clocks has been focused on organs and tissues that have prominent metabolic functions, such as the liver, fat, and muscle. In recent years, skin has emerged as a model for studying circadian clock regulation of cell proliferation, stem cell functions, tissue regeneration, aging, and carcinogenesis. Morphol...
Article
Full-text available
Genome-wide analyses have revolutionized our ability to study the transcriptional regulation of circadian rhythms. The advent of next-generation sequencing methods has facilitated the use of two such technologies, ChIP-seq and RNA-seq. In this chapter, we describe detailed methods and protocols for these two techniques, with emphasis on their usage...
Article
Through the use of bulk measurements in metabolic organs, the circadian clock was shown to play roles in organismal energy homeostasis. However, the relationship between metabolic and circadian oscillations has not been studied in vivo at a single-cell level. Also, it is unknown whether the circadian clock controls metabolism in stem cells. We used...
Article
138-Plat Circadian Metabolic Oscillations in the Epidermis Stem Cells by Fluores- cence Lifetime Microscopy of NADH in Vivo Chiara Stringari 1,2 , Mikhail Geyfman 1 , Hong Wang 1,3 , Viera Crosignani 1 , Vivek Kumar 4 , Joseph S. Takahashi 4 , Bogi Andersen 1 , Enrico Gratton 1 . University California Irvine, Irvine, CA, USA, 2 Laboratory for Optic...
Article
Full-text available
The inbred mouse C57BL/6J is the reference strain for genome sequence and for most behavioral and physiological phenotypes. However, the International Knockout Mouse Consortium uses an embryonic stem cell line derived from a related C57BL/6N substrain. We found that C57BL/6N has a lower acute and sensitized response to cocaine and methamphetamine....
Article
Full-text available
An intriguing study shows that, in epidermal progenitor cells, circadian genes are expressed in successive waves that modulate responses to differentiation signals.
Data
ChIP-seq peak list for USF1.DOI: http://dx.doi.org/10.7554/eLife.00426.015
Data
ChIP-seq peak list for CLOCK.DOI: http://dx.doi.org/10.7554/eLife.00426.016
Data
Oligonucleotide sequences. DOI: http://dx.doi.org/10.7554/eLife.00426.019
Data
Single nucleotide polymorphisms (SNP) in the Suppressor of Clock (Soc) candidate region among 16 mouse strains.DOI: http://dx.doi.org/10.7554/eLife.00426.005
Data
ChIP-seq peak list for BMAL1.DOI: http://dx.doi.org/10.7554/eLife.00426.017
Article
Period determination in the mammalian circadian clock involves the turnover rate of the repressors CRY and PER. We show that CRY ubiquitination engages two competing E3 ligase complexes that either lengthen or shorten circadian period in mice. Cloning of a short-period circadian mutant, Past-time, revealed a glycine to glutamate missense mutation i...
Article
Full-text available
The mammalian circadian clock involves a transcriptional feed back loop in which CLOCK and BMAL1 activate the Period and Cryptochrome genes, which then feedback and repress their own transcription. We have interrogated the transcriptional architecture of the circadian transcriptional regulatory loop on a genome scale in mouse liver and find a stere...
Article
Full-text available
The role of the circadian clock in skin and the identity of genes participating in its chronobiology remain largely unknown, leading us to define the circadian transcriptome of mouse skin at two different stages of the hair cycle, telogen and anagen. The circadian transcriptomes of telogen and anagen skin are largely distinct, with the former domin...
Article
Full-text available
Forward genetic screens have been highly successful in revealing roles of genes and pathways in complex biological events. Traditionally these screens have focused on isolating mutants with the greatest phenotypic deviance, with the hopes of discovering genes that are central to the biological event being investigated. Behavioral screens in mice ty...
Article
Cells possess internal ∼24 hr or circadian clocks that synchronize physiological processes with daily cycles of light and nutrient availability. In this issue, Asher et al. (2010) find that PARP-1 (poly(ADP-ribose) polymerase 1) modifies components of the clock machinery in response to feeding, providing a mechanism for how metabolic rhythms coordi...
Article
Full-text available
Most laboratory mouse strains including C57BL/6J do not produce detectable levels of pineal melatonin owing to deficits in enzymatic activity of arylalkylamine N-acetyltransferase (AANAT) and N-acetylserotonin O-methyl transferase (ASMT), two enzymes necessary for melatonin biosynthesis. Here we report that alleles segregating at these two loci in...
Article
Full-text available
Circadian rhythms in mammals are generated by a transcriptional negative feedback loop that is driven primarily by oscillations of PER and CRY, which inhibit their own transcriptional activators, CLOCK and BMAL1. Current models posit that CRY is the dominant repressor, while PER may play an accessory role. In this study, however, constitutive expre...
Article
Full-text available
Hair follicles undergo recurrent cycling of controlled growth (anagen), regression (catagen), and relative quiescence (telogen) with a defined periodicity. Taking a genomics approach to study gene expression during synchronized mouse hair follicle cycling, we discovered that, in addition to circadian fluctuation, CLOCK-regulated genes are also modu...
Data
Time-course profiles of genes belonging to representative GO Biological Process categories found to be significantly enriched. The heat map was generated using profiling data from the second synchronized hair growth cycle. Expression levels are indicated by colorimetric ratio-scale. Time points are mapped based on histology to the corresponding pha...
Data
Time-course profile clustering of hair-cycle regulated genes. Probe set ID corresponds to the array used for the second and depilation-induced hair growth cycles (Mouse Genome 430 2.0). Old probe set ID corresponds to the array used for the first hair growth cycle (Murine Genome U74Av2).Columns labeled 1–9 correspond to log-transformed, zero-mean g...
Data
Hair cycle staging of Bmal1 knockout mice (−/−) and their control littermates (+/+ and +/−). For each postnatal day (P), mice are grouped by genotype and each mouse is classified into specific phases/stages of the hair growth cycle based on the majority of hair follicles using established morphological guidelines. In general, we noted a slightly mo...
Data
Probabilistic model for detection of periodic profiles. (4.01 MB PDF)
Data
Exclusion of gene expression changes that correspond to tissue composition changes. (A) Expression profiles of marker genes that are altered as the tissue composition changes during the hair growth cycle. The marker genes for the different cell types are as follows: filaggrin and loricrin for the cornified cells, keratin 1 and 10 for the suprabasal...
Data
Expression of circadian clock genes from laser capture microdissected skin compartments. Q-PCR of Bmal1 (A), Per2 (B) and Cry2 (C) from LCM-hair follicles, dermis, and epidermis for telogen and late anagen dorsal skin at ZT10 and ZT18/ZT2. (D) Q-PCR of Dbp from laser capture microdissected hair follicles at telogen, early anagen (anagen I–II), mid...
Data
List of genes previously reported to have hair cycle-dependent gene expression changes. Probe set ID corresponds to the array used for the second and depilation-induced hair growth cycles (Mouse Genome 430 2.0). Old probe set ID corresponds to the array used for the first hair growth cycle (Murine Genome U74Av2). pHC is the posterior probability of...
Data
Hair cycle staging of Clock mutant mice (Cl/Cl) and their control littermates (+/+ and Cl+). Methodology same as Table S3. (0.06 MB PDF)
Data
Expression of circadian clock genes and proteins in mouse dorsal skin at different phases of the hair growth cycle. (A) In situ hybridization staining of telogen, early anagen, late anagen, and catagen dorsal skin at ZT10 with Bmal1 (left column) and Dbp (right column) anti-sense probes. Note the black pigment of the hair shaft in late anagen hair...
Data
No morphological abnormalities in skin and hair follicle in Clock and Bmal1 mutant mice. (A) Hair follicle structures are normal in Clock and Bmal1 mutant mice. The top row show the H&E sections of hair follicles in dorsal skin of Clock and Bmal1 mutant mice and their control littermates at late anagen. The bottom three rows are the corresponding i...
Article
The success of forward genetic (from phenotype to gene) approaches to uncover genes that drive the molecular mechanism of circadian clocks and control circadian behavior has been unprecedented. Links among genes, cells, neural circuits, and circadian behavior have been uncovered in the Drosophila and mammalian systems, demonstrating the feasibility...
Article
Using a forward genetics ENU mutagenesis screen for recessive mutations that affect circadian rhythmicity in the mouse, we isolated a long period (approximately 26 hr) circadian mutant named Overtime (Ovtm). Positional cloning and genetic complementation reveal that Ovtm is encoded by the F-box protein FBXL3, a component of the SKP1-CUL1-F-box-prot...

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