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New genes related to autism spectrum disorder

Researchers at the University of Barcelona have identified new genes in the BEX/TCEAL cluster that are related to autism spectrum disorder and other neurological diseases. The study used animal models to describe molecular mechanisms involved in the development of the neocortex in humans and other placental mammals.

SourceUniversity of Barcelona·JournalGenome Biology·DateOct 26, 2020

Breaking the silence: scientists investigate epigenetic impact across whole genome

Researchers at OIST Graduate University have identified previously unknown sections of DNA that are silenced by epigenetic regulation in plant cells. The study reveals a crucial role of these sites in suppressing the activity of disruptive 'jumping genes' called transposons, which can threaten genome integrity.

Renegade genes caught red handed

Researchers dispute the long-held belief that heterochromatin is a reliable guardian of the human genome. A study by University of Arizona researcher Keith Maggert reveals that heterochromatin can flicker on and off, allowing transposons to cause mutations and damage. This instability has significant implications for our understanding ...

SourceUniversity of Arizona·JournalProceedings of the National Academy of Sciences·DateSep 16, 2019

Smuggling route for cells protects DNA from parasites

Cells use a molecular safety mechanism to smuggle genetic information molecules around the cell, which are then used to recognize and shut down parasites. This discovery provides new insight into how animal genomes defend themselves against DNA parasites and reveals a previously unknown RNA transport route.

SourceAarhus University·JournalCell·DateAug 9, 2019

Expansion of transposable elements offers clue to genetic paradox

A recent study reveals that transposable element insertions drive rapid phenotypic variation in plants, enabling them to adapt to novel environments. Researchers found that transposable elements are enriched in the gene promoter regions of a plant species with limited genetic variation, associated with changes in gene expression.

SourceChinese Academy of Sciences Headquarters·JournalProceedings of the National Academy of Sciences·DateMar 17, 2019

New techniques better determine how ancient viral DNA influences human genes

Researchers have developed new techniques to identify which of our genes are influenced by ancient viral DNA snippets, revealing complex interactions between viruses and human genetic material. The study found that a single transposon can control multiple genes, increasing the complexity of its impact on health and disease.

Jumping genes shed light on how advanced life may have emerged

Researchers discovered that retrotransposons and nonhomologous end-joining (NHEJ) interacted to create a selection pressure that helped lead to the emergence of advanced life. This interaction enabled eukaryotes to mix and match genes, creating more complicated functions.

SourceCarl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign·JournalProceedings of the National Academy of Sciences·DateNov 19, 2018

Preventing a genetic uprising in early life

A recent study published in Cell Stem Cell has discovered a mechanism to prevent genetic chaos caused by transposons in early human development. The research found that endosiRNAs, a type of small interfering RNA, play a crucial role in regulating transposon activity during epigenetic reprogramming.

SourceBabraham Institute·JournalCell Stem Cell·DateNov 2, 2017

Genetic advance for male birth control

Researchers at Michigan State University have identified the PNLDC1 gene as a key player in regulating sperm production, providing a genetic foundation for male birth control. The study's findings suggest that silencing this gene can lead to infertility in mice, making it a promising approach for human male contraception.

SourceMichigan State University·JournalNature Communications·DateOct 10, 2017

Repetitive elements shape embryonic chromatin landscape

Scientists from Helmholtz Zentrum München have found that retrotransposons, particularly LINE1 elements, regulate global chromatin accessibility in the early mouse embryo. This study identifies a novel role for retrotransposons in shaping the chromatin landscape necessary for correct developmental programming.

Tracking down the jumping genes of maize

Researchers at UC Davis and Cold Spring Harbor Laboratory have mapped the 'jumping genes' of maize, identifying transposable elements that regulate gene expression and impact plant traits. The new genome sequence enables a deeper understanding of the complex relationships between these elements and the diversity of the genome.

Decoding of tarsier genome reveals ties to humans

The tarsier genome analysis confirms that tarsiers belong to the dry-nosed primate category, sharing recent transposon families with humans and bushbabies. The study also identified 192 genes linked to the tarsiers' unique traits, which may be associated with human diseases.

SourceWashU Medicine·JournalNature Communications·DateOct 6, 2016

Study results advance 'transposon theory of aging'

A new study strengthens the links between transposons and aging, showing that increased transposon activity correlates with decreased lifespan in fruit flies. The study also reveals that manipulating genes involved in heterochromatin repression can lengthen lifespan, suggesting a potential therapeutic target for age-related diseases.

SourceBrown University·JournalProceedings of the National Academy of Sciences·DateSep 12, 2016

Tight DNA packaging protects against 'jumping genes,' potential cellular destruction

Researchers at UNC School of Medicine discovered that tight DNA packaging in chromosomes mainly guards against virus-like genetic elements known as transposons or 'jumping genes,' which can copy and paste themselves throughout the genome, potentially destroying important genes. The discovery clarifies the role of heterochromatin and ad...

SourceUniversity of North Carolina Health Care·JournalGenes & Development·DateSep 1, 2016