Articles tagged with Gene Expression
A study published in Experimental Physiology found that short-sleepers have lower blood levels of three microRNAs, which influence gene expression and maintain vascular health. This could lead to new tests for sleep-deprived patients concerned about their health.
Research reveals that male fruit flies' genitals remain preserved in size even when food is scarce, allowing them to reproduce more successfully. This preservation is linked to lower levels of a growth factor called FOXO, which acts as a brake on growth and size maintenance.
Researchers at Tokyo Medical and Dental University use genome editing to create a human stem cell model of congenital hepatic fibrosis, uncovering molecular players that contribute to the illness. They identify IL-8 and CTGF as key genes involved in the disease's progression.
Researchers developed an algorithm called Scanorama that merges over 20 diverse human cell datasets into a single, diverse source of data. The algorithm uses a modified computer-vision technique to find matching cells across datasets and preserves unique cell types.
MIT researchers develop a method to extract comprehensive samples of massive cell datasets, preserving rare cell types and their biological information. The 'sketching' approach generates compact summaries of large datasets in minutes, making it practical for biological studies.
The WINTHER trial successfully matched personalized therapy to 35% of patients with advanced cancer, showing improved overall survival for those with a high degree of matching. The trial's strategy employed RNA expression testing to tailor treatment based on gene expression differences between tumors and normal tissues.
A study found that exercise-induced cognitive improvements can be inherited by offspring via sperm. Exercise has been shown to increase the growth of immature neurons and improve mitochondrial function in the brain, leading to enhanced memory performance.
BRB-seq, a novel approach to RNA sequencing, preserves strand-specificity and detects the same number of genes as gold standard methods. The technique is 25 times less expensive than commercial RNA sequencing technologies, enabling bulk RNA sequencing of large sets of samples.
Researchers identified unique genetic signatures in patients with active celiac disease and those in remission, revealing differences in gene expressions. The study uncovered potential targets for therapeutic intervention and shed light on the underlying mechanisms of celiac disease.
Researchers at the University of Otago and Indian Statistical Institute have discovered distinct epigenetic markers in oral cancer tissues that are associated with patient survival. The findings, published in the journal Epigenomics, could help save thousands of lives by identifying cancer cells early.
Long-term spaceflight causes significant changes to gene expression, immune system, and DNA repair systems. The study provides insights into the effects of prolonged space travel on astronaut health and may help scientists develop treatments or prevention strategies.
Researchers found that male fruit flies produce fewer proteins in their seminal fluid when females are without competition, leading to health disadvantages for the females. In contrast, polygamous males with no competition can manipulate females through protein receipt, increasing their own reproductive success.
A recent study published in JNeurosci has identified genes and molecular pathways associated with higher educational attainment in older adults. The research found that individuals with higher education levels had thicker prefrontal brain regions, which are linked to improved working memory and decision-making.
The Slide-seq technique generates detailed three-dimensional maps of tissues, revealing the location and activity of cell types and genes. This platform offers unparalleled views of tissue function, allowing researchers to study cellular relationships, gene expression, and responses to perturbations.
Researchers have developed a new method to study gene expression and its relationship with cell behavior, including regeneration. The method, called single-cell-digital gene expression (1cell-DGE), allows for the analysis of RNA from individual living cells in intact tissue without compromising positional information.
A new study found that endocrine disruptors can alter female reproduction and sexual development in offspring, affecting reproductive health throughout multiple generations. The researchers observed delayed puberty, abnormal cycles, and ovulation in third- and fourth-generation females.
A new study published by the Moskalev Lab has revealed how overexpressing the pro-longevity gene Gclc in Drosophila melanogaster leads to life extension and changes in the thorax's transcriptome, including genes involved in metabolism, immune system, and circadian rhythmicity.
Daniel Hartl receives the 2019 Thomas Hunt Morgan Medal for his influential contributions to experimental and theoretical genetics research, combining mathematical models with cutting-edge techniques. His work explains how DNA mutations are passed through generations, influencing species divergence.
Scientists at Cold Spring Harbor Laboratory have created a ranked list of genes that are likely to be involved in any disease, allowing researchers to distinguish between these 'usual suspects' and those unique to specific conditions. The study's findings provide valuable context for interpreting gene activity in disease onset.
Research reveals that symbiotic bacteria in Hawaiian bobtail squid alter gene expression in the eye and gill organs, with effects varying by time of day. Bioluminescence may drive system-wide changes in gene expression.
Gene activity in defenders reflects origin of attacking slavemakers, with successful invaders triggering weaker defenses. Researchers found that host ants react aggressively to rare slave-makers and not to common ones, highlighting the complex co-evolutionary relationship between parasites and their hosts.
A team of researchers led by Joshua Sanes created the first cellular atlas of the primate retina, identifying 65-70 separate cell types and their expressed genes. The study sheds light on the mechanisms that give rise to differences in foveal cells and offers a foundation for understanding vision-related diseases.
Researchers at the Allen Institute have created the largest single-cell database of mammal organ development, tracing gene expression from a single cell to fully formed organs. The study provides valuable insights into human biology and developmental diseases, with potential applications in understanding common adult diseases.
Research in zebrafish reveals that clock genes determine daily behavioral rhythms and activity levels. The study found that eliminating these genes reduces energy supply, leading to lower locomotion and more resting behavior.
A new study found that warmer water temperatures combined with low-level chemical exposure influence the expression of genes in the offspring of a North American fish species. The finding threatens organisms sensitive to water temperature and highlights the need for reevaluating regulatory decisions based on short-term testing.
A KAIST team has developed a noninvasive light-sensitive photoactivatable recombinase suitable for genetic manipulation in vivo. The new tool enables spatiotemporal control of gene expression in the mouse brain with high precision and minimal side effects.
Researchers discovered 677 genes and small RNAs expressed differently between African and global Salmonella strains, leading to alterations at the protein level. The study provides a powerful tool for understanding the bacteria's genetic basis and potential antibiotic resistance.
A study of wild baboons in Kenya found that high-ranking individuals have better access to resources and immune system genes. However, the relationship between social status and health differs between males and females, suggesting a sex-specific connection between rank and immune function.
A study found that random differences in gene expression during fetal development can lead to a survival advantage, potentially contributing to adult health issues. The researchers propose that these epigenetic variations can become more common in individuals exposed to famine or adverse conditions during gestation.
A new study finds that spinal cord injuries profoundly impact the body's internal clocks, affecting body temperature, hormone fluctuations, immunity, and other bodily processes. The researchers discovered that expression of clock genes was reduced in both injured and uninjured tissue, with implications for recovery.
Myasthenia gravis is a chronic autoimmune disorder that causes weakening of skeletal muscles. Researchers at Kanazawa University found that the immune system regulatory molecule programmed cell death ligand 1 (PD-1) is abundant in muscle tissue of patients, which may help reduce disease symptoms.
Researchers used single-cell RNA sequencing to study gene expression in individual cells and identify unique therapeutic targets for cancers that form in specific cell types. The study found that mutations in certain genes can make cells vulnerable to apoptosis, providing a potential way to prevent or treat cancer.
Neuroscientists at the Allen Institute have sorted brain cells from the cerebral cortex into 133 different cell types based on their gene expression patterns. This comprehensive study provides a detailed catalog of brain cell types and lays the groundwork for understanding their functions.
Researchers at UC Santa Cruz have discovered that sperm retain epigenetic marks important for the development of the germ line in offspring. This study provides evidence that the life experience of a father can affect the health of his descendants, highlighting the importance of epigenetic information carried by sperm.
The study found that pro-inflammatory TNFα and anti-inflammatory CCL18 cytokines are increased in human atherosclerotic lesions, associated with cholesterol accumulation. The expression levels vary across plaque stages, with maximum levels in lipofibrous plaques.
Researchers identified specific genes and cells associated with CKD, including the adaptor protein DAB2 in the TGF-β pathway. Further experiments confirmed that reducing DAB2 expression protected mice from CKD. The findings could inform treatment options for this complex disease.
A new Cornell University-led study has identified genes that were altered in tame animals in two areas of the brain involved with learning and memory. Genes impacting serotonergic and glutaminergic neurons, important for learning and memory, were clearly affected by selection toward tameness.
Scientists at the Francis Crick Institute developed machine learning algorithms to predict yeast metabolism from protein content, shedding light on the complex relationships between enzymes and metabolites. This breakthrough could lead to the creation of perfect beer flavors and personalized treatments for metabolic disorders.
A new study suggests that paternal diet influences offspring health by affecting sperm DNA methylation tags and seminal plasma immunological responses. Mice fed a low-protein diet had overweight offspring with dysfunctional metabolism, highlighting the importance of a healthy father's nutrition for child well-being.
Gene therapy using optimized AAV to deliver human factor VIII showed substantial hFVIII expression and no detectable antibody response in cynomolgus macaques. The results suggest that AAVhu37-based gene therapy has the potential to advance to clinical trials for treating hemophilia A.
The international team of researchers presents the first high-quality fully annotated reference genome sequence of bread wheat variety Chinese Spring. This advancement provides a powerful tool for accelerating the development of new wheat varieties designed to address human nutrition and crop resiliency needs.
Researchers have successfully engineered silkworms to produce high yields of spider silk using genome editing, a breakthrough that could pave the way for mass production of this versatile material. The transgenic silkworms produced fibers with improved elasticity and extensibility compared to wild-type silkworms.
Gene expression analysis of blood samples from 15 kidney transplant recipients revealed that the most robust gene expression changes occurred in the first day following transplantation. A comparison between living donors and deceased donor groups identified 11 genes that may play a key role in kidney repair and regeneration.
A subset of dopaminergic neurons are inhibited during the day by light-responsive neuropeptide Pigment Dispersing Factor (PDF) and its receptor (PDFR), promoting wakefulness. High daytime levels of PDF increase daytime sleep, while reducing PDFR expression decreases daytime sleep.
Researchers found that nanoplastics caused damage to the DNA and cell membranes of mussels, leading to oxidative stress and changes in gene expression. The study highlights the potential long-term consequences of consuming mussels contaminated with nanoplastics.
Researchers have identified a protein called dMLL3/4 that helps balance out differences between chromosomes inherited from parents. This discovery may lead to new diagnostic approaches and improved embryo culture media formulations for assisted reproduction techniques.
Researchers at the University of Arizona College of Medicine - Phoenix are developing a quick and accurate diagnostic test for radiation exposure in case of a nuclear disaster. The test uses gene expression biomarkers to calculate the amount of radiation absorbed by the human body, potentially saving thousands of lives.
Researchers developed a personalized Therapeutic Intervention Fingerprint (pTIF) to predict the effectiveness of targeting specific biological factors for controlling neurological disease progression. This technique can categorize patients with their unique physiological needs, leading to more effective and tailored treatments.
Researchers successfully used CRISPR-Cas9 genome editing to restore normal levels of the AAT enzyme in mouse models of alpha-1 antitrypsin deficiency. The approach showed promise for treating patients with this genetic disorder.
A recent study published in the American Journal of Human Biology found that healthy gaming experiences are linked to favorable gene expression profiles. The research, led by Dr. Jeffrey Snodgrass, highlights the importance of social connectedness in mitigating negative effects of online gaming.
A study by a Danish-German research team reveals that modified RNA bases play a crucial role in controlling gene expression from DNA to functional RNA. The researchers used a newly developed technique to label newly made RNA with the m6A modification, demonstrating its impact on RNA maturation and splicing efficiency.
A team of scientists developed a high-throughput approach to integrate laboratory experiments, literature data, and network analysis to study Huntington's disease. The approach revealed that changes in inflammation, cell architecture, and calcium signaling drove the disease forward, while counteracting these changes improved health.
Researchers have found a blood-based genetic biomarker, KLRD1, which determines an individual's susceptibility to the flu. Those with higher levels of this gene have better immune defenses and are less likely to fall ill.
Researchers found that a type of lung cancer's spread is facilitated by immune cells forming clots in tumors. These clots allow tumor cells to migrate and spread to other parts of the body. The study identifies a new target for potential metastasis treatment.
Juhyun Lee is using a new $251,000 grant from the American Heart Association to explore targeted delivery of messenger RNA to reverse damage caused by congenital heart disease. His goal is to modulate mechanical forces and reduce gene expressions to stimulate heart growth or healing.
Researchers found that inheriting a variation in the PM20D1 gene increases the risk of developing Alzheimer's disease, making it an excellent candidate for clinical prevention trials. The study highlights the importance of international scientific collaboration and multidisciplinary research to tackle complex diseases like dementia.
Researchers developed a method to improve electrical transmission in the heart by introducing the Connexin 43 gene into cells forming the infarct scar. Mice with overexpressed Cx43 showed reduced cardiac arrhythmias compared to control animals.
EPFL scientists have joined the Human Cell Atlas initiative, a global project mapping every type of cell in the human body. The team developed an automated single-cell analysis pipeline, enabling non-expert labs to engage in high-level genomic research.
Researchers discovered that HTLV-1 survives by evading immune surveillance through transient Tax expression in infected cells. This unique strategy allows the virus to maintain a population of infected leukemic cells, making it a potential target for new therapies.
Researchers have detailed for the first time how interneurons emerge and diversify in the brain, tracing their lineage from earliest precursor states to mature forms in mice. The study identified key genetic programs that determine the fate of developing interneurons, shedding light on their functions and potential treatment strategies.