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Babraham Institute


Genetic DJ: Growing cells remix their genes

A study by Babraham Institute and Weizmann Institute reveals genes are constantly rearranged in cells, changing their positions to fine-tune gene expression. Researchers collected data from over 4,000 individual cells using single-cell Hi-C technology, providing unique insights into genome organisation.

SourceBabraham Institute·JournalNature·DateJul 5, 2017

Mapping genes could improve cancer diagnosis

Researchers have developed a new method to detect genetic changes in cancer cells using Hi-C, which can identify major genome rearrangements and copy number variations with high accuracy. This approach has the potential to aid targeted treatments and enhance cancer diagnosis.

SourceBabraham Institute·JournalGenome Biology·DateJul 4, 2017

Tick tock, stay ahead of the aging clock!

Researchers at Babraham Institute and European Bioinformatics Institute identified a mouse epigenetic ageing clock, which shows age-related changes in DNA methylation. The accuracy of the mouse clock is surprisingly similar to humans, with lifestyle interventions affecting ticking rate.

SourceBabraham Institute·JournalGenome Biology·DateApr 12, 2017

A tale of 2 states

Human embryonic stem cells exist in two states: naïve and primed. Researchers have identified molecular flags on these cells, allowing them to track and investigate their transition. This approach has revealed new insights into the timing and coordination of gene activity changes during reprogramming.

SourceBabraham Institute·JournalCell Stem Cell·DateMar 23, 2017

Aging can be good for you (if you're a yeast)

Research in yeast reveals increased adaptability with age, benefiting growth on alternative food sources like galactose. This study challenges the notion of aging as an inevitable process, suggesting potential benefits and ancient mechanisms that may be conserved in more complex organisms.

SourceBabraham Institute·JournalAging Cell·DateMar 1, 2017

Understanding X-chromosome silencing in humans

Scientists have discovered a new long RNA molecule, XACT, which accumulates with XIST on active X-chromosomes in human embryos. This finding explains why XIST is unable to trigger X-chromosome silencing until later stages of development. The research also reveals that XACT restrains XIST activity before chromosome silencing occurs.

SourceBabraham Institute·JournalCell Stem Cell·DateDec 15, 2016

A change of heart

Cardiac diseases cause pathological growth leading to heart failure. Researchers found epigenetic marks responsible for this growth are lost in disease, allowing cells to switch back to fetal form and leading to irregular rhythms. This finding points to a new strategy for epigenetic therapy.

SourceBabraham Institute·JournalJournal of Clinical Investigation·DateNov 28, 2016

Vitamins A and C help erase cell memory

Researchers discovered vitamins A and C enhance epigenetic memory erasure by increasing TET enzyme activity, a crucial step for regenerative medicine. The study provides insights into the mechanisms of vitamin A and C action, with potential implications for treating vitamin A-resistant acute promyelocytic leukemia.

SourceBabraham Institute·JournalProceedings of the National Academy of Sciences·DateOct 12, 2016

Autophagy under the microscope as never before

Scientists have dissected the autophagy process in unprecedented molecular detail using live imaging and super resolution microscopy. The study reveals how the first autophagy structure forms and clarifies protein and membrane associations leading to its development into a fully-fledged autophagosome.

SourceBabraham Institute·JournalNature Communications·DateAug 11, 2016

Stem cells know how to open up and unwind

Research found that heterochromatin organisation in embryonic stem cells is maintained in an open form through the action of key stem cell factors. This open architecture may contribute to keeping stem cells unspecialised and full of developmental potential.

SourceBabraham Institute·JournalGenes & Development·DateApr 28, 2016

The importance of resting phases in B cell development

Researchers discovered that B cells rely on RNA binding proteins ZFP36L1 and ZFP36L2 to induce quiescence, allowing them to 'rest up' between developmental events. This mechanism is crucial for proper B cell development, as seen in mice where a 98% reduction of mature B cells was observed when these proteins were absent.

SourceBabraham Institute·JournalScience·DateApr 21, 2016

Mom's in control -- even before you're born

Researchers have discovered that epigenetic information in the egg plays a crucial role in shaping the development of the placenta during pregnancy. The study found that DNA methylation marks from the egg are essential for correct placental development, particularly in regulating cell adhesion and migration.

SourceBabraham Institute·JournalDevelopmental Cell·DateJan 25, 2016

Come here and be quiet!

A novel technique identified an unusually strong 3D network of developmental genes in ESCs, physically clustered and silenced by Polycomb repressive complex (PRC1) to maintain the undifferentiated state. This mechanism allows for selective release of genes, controlling early development decisions.

SourceBabraham Institute·JournalNature Genetics·DateAug 31, 2015

Joining the genomic dots

A new technique called Promoter Capture Hi-C was used to connect regulatory elements in the mouse and human genomes, providing insight into how genes are regulated. The analysis identified long-range interactions between promoters and enhancers, shedding light on the genetic basis of disease.

SourceBabraham Institute·JournalNature Genetics·DateMay 4, 2015