When they analyzed microbes found in fecal samples collected from
mice and humans at different times of day, they discovered rhythmic fluctuations in the abundance of microbes and their biological activities.
«This is the first systematic comparison of
the mouse and human at the genomic level,» said Bing Ren, Ph.D., co-senior author on the Consortium's main Nature study and professor of cellular and molecular medicine at the University of California, San Diego.
Not exact matches
Genetics has revealed that related molecular timepieces are
at work in fruit flies,
mice and humans
Compared with
mice with cells from healthy people as well as non-chimera
mice, those whose brains had
human schizophrenia cells were more afraid to explore a maze, more anxious, more antisocial, less able to feel pleasure (from sipping sugar water), worse
at remembering,
and more sleepless — all of which characterize people with schizophrenia, too.
A study by researchers
at the University of Chicago Medicine shows that when
mice that are genetically susceptible to developing inflammatory bowel disease (IBD) were given antibiotics during late pregnancy
and the early nursing period, their offspring were more likely to develop an inflammatory condition of the colon that resembles
human IBD.
«Our study shows that epigenetic drift, which is characterized by gains
and losses in DNA methylation in the genome over time, occurs more rapidly in
mice than in monkeys
and more rapidly in monkeys than in
humans,» explains Jean - Pierre Issa, MD, Director of the Fels Institute for Cancer Research
at LKSOM,
and senior investigator on the new study.
Researchers
at Weill Cornell Medical College recently identified a gene abnormality that is associated with anxiety - related behaviors; it makes
humans and mice hypervigilant to cues that signal danger.
«Our research is the first to study Zika infection in a
mouse model that transmits the virus in a way similar to
humans,» explains Alysson R. Muotri, Ph.D., professor
and director of the Stem Cell Program
at UC San Diego
and co-senior author of the study.
The
mouse, dog
and human genomes are of high quality whereas the three others are
at different stages of analysis completion.»
The book looks
at fish that live in subfreezing waters, ruminating monkeys, ridiculously poisonous newts, birds that see in the ultraviolet,
mice that live on lava flows, cave fish, coelacanths, bush babies,
humans,
and some other marvels of evolution.
«Finding these similarities
and studying the aspects of
mouse biology that may reflect
human biology, allows us to approach the study of
human illnesses in a better way,» affirms Bing Ren, one of the principal authors from the ENCODE Consortium
and a lecturer in molecular
and cellular medicine
at the University of California — San Diego.
Géléoc
and colleagues
at Boston Children's Hospital studied
mice with a mutation in Ush1c, the same mutation that causes Usher type 1c in
humans.
Molecular geneticist Cheng Chi Lee, developmental biologist Gregor Eichele,
and their co-workers
at the Baylor College of Medicine in Houston have isolated a gene in
mice and humans that shares 44 % of the amino acid sequence of the period (per) gene of the fruit fly Drosophila melanogaster.
The large amounts of fat around the testes of obese
mice, «could alter the environment
and encourage epigenetic changes», says Teague, who presented the results
at the 14th World Congress on
Human Reproduction in Melbourne, Australia, this month.
An additional study, currently available
at bioRxiv, led by the researchers from the CRG
and Cold Spring Harbour Laboratory, highlights the fact that a substantial part of
human and mice genes have maintained an essentially constant expression throughout evolution, in tissues
and various organs.
Senior author Madhav Dhodapkar, M.D., the Arthur H.
and Isabel Bunker Professor of Medicine
and Immunobiology,
and chief of Hematology, said the study, using tissue
and blood samples from
humans and mice, shows that chronic stimulation of the immune system by lipids made in the context of inflammation underlies the origins of
at least a third of all myeloma cases.
This is the finding of a study in both
mice and human patients led by researchers
at NYU Langone Medical Center
and published online June 9 in the journal Cell.
«Even the timing of the emergence of symptoms in the
mice — during young adulthood — parallels the onset of schizophrenia in
humans,» said Joseph Gogos, PhD, a professor of physiology
and neuroscience
at CUMC, a principal investigator
at the Zuckerman Institute
and a lead author of the paper.
Using the new gene - editing enzyme CRISPR - Cpf1, researchers
at UT Southwestern Medical Center have successfully corrected Duchenne muscular dystrophy in
human cells
and mice in the lab.
At a neuroscience meeting, two teams of researchers will report implanting
human brain organoids into the brains of lab rats
and mice, raising the prospect that the organized, functional
human tissue could develop further within a rodent.
In addition to looking
at mouse models of diabetes, the researchers also showed that exposure of
human pancreatic islet cells — both from healthy donors
and from patients with Type 1 diabetes — to fasting - mimicking diet in a dish stimulated insulin production.
Judy Anderson, a muscular dystrophy expert
at the University of Manitoba in Winnipeg, Canada, adds that evidence for acetylcholine defects in
human muscular dystrophy has been contradictory over the years, but if this preliminary finding holds up in
mice and humans, it could pave the way for new drug targets.
«There's a lot of grumbling, both in the general public
and the scientific community, about how often we cure diseases in
mice that never translates when we try those cures in
humans,» says Felipe Sierra, director of the Division of Aging Biology
at the National Institute on Aging.
Mice without the leptin gene, called ob / ob, overeat, weigh in
at three to four times normal,
and develop symptoms similar to the obesity - related diabetes seen in
humans.
Kristen Earle, Gabriel Billings, KC Huang
and Justin Sonnenburg, of Stanford University's School of Medicine, Department of Microbiology
and Immunology, took second place with this photo of a
mouse colon colonized with
human microbiota, seen
at 63x.
Dr. Aplin
and Jessica Teh, PhD, his senior postdoctoral researcher
at Jefferson (Philadelphia University + Thomas Jefferson University), examined the effects of a combination of two FDA - approved targeted agents on
human melanomas grafted onto
mice.
Using the supercomputers
at Almaden
and Lawrence Livermore National Laboratory, the group simulated networks that crudely approximated the brains of
mice, rats, cats
and humans.
«For example, cancer research is heavily reliant on
mouse models,
and as a result we've become very good
at curing
mice, but that hasn't translated very well to
humans.
In a paper publishing August 7th in the Open Access journal PLOS Biology, researchers
at the Max Planck Institute of Molecular Cell Biology
and Genetics (MPI - CBG) succeeded in mimicking the sustained expression of the transcription factor Pax6 as seen in the developing
human brain, in
mouse cortical progenitor cells.
However, if a softer noise (known as a prepulse) is played before the loud tone,
mice and humans are «primed»
and startle less
at the second, louder noise.
Joseph Castellano
at Stanford University in California
and his colleagues discovered this by collecting blood from people
at three different life stages — babies, young people around the age of 22,
and older people around the age of 66 —
and injecting the plasma component into
mice that were the equivalent of around 50 years old in
human years.
The results obtained by Afsaneh Gaillard's team
and that Pierre Vanderhaeghen
at the Institute of Interdisciplinary Research in
Human and Molecular Biology show, for the first time, using
mice, that pluripotent stem cells differentiated into cortical neurons make it possible to reestablish damaged adult cortical circuits, both neuroanatomically
and functionally.
Working with
human breast cancer cells
and mice, scientists
at The Johns Hopkins University say new experiments explain how certain cancer stem cells thrive in low oxygen conditions.
A common antioxidant found in
human breast milk
and foods like kiwi fruit can protect against nonalcoholic fatty liver disease (NAFLD) in the offspring of obese
mice, according to researchers
at the University of Colorado Anschutz Medical Campus.
Before Katlyn showed up
at NIH, the doctors there were already well prepared: They had inserted healthy
human ADA genes into a modified
mouse retrovirus — a type of virus that can enter
human cells
and transfer new genetic material right into the DNA strands in their nuclei.
They found evidence of Del - 1 in the same areas as osteoclast activity, then followed up by generating
human and mouse osteoclasts in vitro
and found Del - 1 mRNA
and protein expressed
at high levels.
MLVs so dependably cause cancer in lab - bred
mice — especially leukemia
and lymphoma — that a small fraternity of scientists
at the NCI
and elsewhere has fruitfully studied these viruses since the 1960s in an effort to understand how
human cancer begins.
In marked contrast to the widely held notion that the insulin - producing pancreatic beta cell loses function with wear
and tear, the researchers now show that
mouse and human beta cells are fully functional
at advanced age.
Starting in the mid-2000s, Yoshiki Sasai's team
at the RIKEN Center for Developmental Biology in Kobe, Japan, demonstrated how to grow brainlike structures using embryonic stem cells, first from
mice and then
humans.
Now, a new study in
mice shows how a gene, called FOXP2, implicated in a language disorder may have changed between
humans and chimps to make learning to speak possible — or
at least a little easier.
But Husseini Manji, head of neuroscience research
and development
at Janssen Pharmaceutical Companies in Titusville, New Jersey, cautions against assuming that results in
mice will bear out in
humans.
«The methods for achieving transplantation tolerance differ between
mice and humans, but the mechanisms that maintain it are likely shared,» said Marisa Alegre, MD, PhD, professor of medicine
at the University of Chicago
and co-senior author on the study.
«These results are especially exciting because they show that we can take findings in the
mouse and possibly apply them
at the
human patient population,» said Koenig.
Similar to
humans, the
mice developed tumors
at secondary sites including the liver, lung, peritoneum,
and diaphragm.
By studying how these genes cause defects in fly
and mouse models, we can improve our insights into the mechanisms related to
human disease,» said corresponding author
and Dr. Hugo J. Bellen, professor of neuroscience
and molecular
and human genetics
at Baylor College of Medicine
and an investigator
at the Howard Hughes Medical Institute.
«By identifying the signals that instruct
mouse progenitor cells to become cells that make tubes
and later insulin - producing beta cells, we can transfer this knowledge to
human stem cells to more robustly make beta cells, says Professor
and Head of Department Henrik Semb from the Novo Nordisk Foundation Center for Stem Cell Biology
at the Faculty of Health
and Medical Sciences.
• Piero Anversa
at New York Medical College in Valhalla, New York,
and Donald Orlic
at the National
Human Genome Research Institute in Bethesda, Maryland, used
mouse bone marrow to repair damaged
mouse hearts.
In a novel animal study design that mimicked
human clinical trials, researchers
at University of California, San Diego School of Medicine report that long - term treatment using a small molecule drug that reduces activity of the brain's stress circuitry significantly reduces Alzheimer's disease (AD) neuropathology
and prevents onset of cognitive impairment in a
mouse model of the neurodegenerative condition.
«Worms,
mice,
humans,
and even fruit flies show similar effects of intoxication
at similar alcohol concentrations,» he says,
and human neurons contain a switch similar to that in C. elegans.
UBC Psychiatry Professor Dr. Weihong Song
and Neurology Professor Yan - Jiang Wang
at Third Military Medical University in Chongqing attached normal
mice, which don't naturally develop Alzheimer's disease, to
mice modified to carry a mutant
human gene that produces high levels of a protein called amyloid - beta.