Genetics & Molecular Biology

Cellular structures called microtubules are tagged with a variety of chemical markers that can influence cell functions and the pattern of these markers makes up the "tubulin code". One of the main writers of this code is tubulin tyrosine ligase-7 (TTLL7), according to a new paper. 

Researchers have discovered a gene, which they have named ICARUS1,  that enables plants to regulate their growth in different temperatures, and it could lead to new ways of optimizing plant growth in different climates.

Photosynthesis, the process by which plants utilize the sun's energy to create their own, leaves behind a unique calling card in the form of a chemical signature that is spelled out with stable oxygen isotopes.

Photosynthesis by microscopic plants forms the base of the oceanic food chain, but it is difficult to measure how productive these plants are in natural settings. This research will make it easier to do so.

Most oxygen atoms contain eight protons and eight neutrons and are represented by the symbol O-16. More than 99.9 percent of Earth's oxygen is O-16, but two heavier oxygen isotopes exist in trace amounts: O-17, with one extra neutron, and O-18, with two.

Mutations in two genes cause a fatal lung scarring disease known as familial pulmonary fibrosis and can cause excessive shortening of the ends of chromosomes, known as telomeres. Telomeres are repetitive sequences of DNA that protect the ends of chromosomes from deteriorating. Think of them like the plastic ends of shoelaces, which protect shoelaces from fraying. 

One of developmental biology's biggest mysteries is ontogeny and the signals that transform masses of undifferentiated cells into tremendously complex organisms. 

A new paper suggests that it all begins with a single "master" growth factor receptor,  nuclear Fibroblast Growth Factor Receptor 1 (nFGFR1), that regulates the entire genome.  The research using mouse embryonic stem cells hopes to challenge the supposition that specific types of growth factors only functioned at a cell's surface and that growth factors function from within the nucleus.

When the chemotherapy drugs like cisplatin or oxaliplatin hit cancer cells, they damage DNA so that the cells can't replicate but those cells have ways to repair the DNA and so the cancer drugs aren't as effective as they could be.

When DNA is damaged, cells use many enzymes to cut the strand of DNA and excise the damaged fragment. Then, other enzymes repair the original DNA so that the cells can function properly. Previously, Sancar's lab used purified enzymes to discover how this process happens in DNA damaged by UV irradiation and by chemotherapeutic drugs such as cisplatin and oxaliplatin.

"Organoids", a futuristic-sounding term for three-dimensional cultures derived from tumors of cancer patients, closely replicate key properties of the original tumors - so close that these "organoid" cultures could be used for large-scale drug screens for the detection of genetic changes associated with drug sensitivity and pave the way for personalized treatment approaches. 

We all know how irritating it is to have an inbox flooded with junk mail.

Fortunately email providers these days contain filters to keep the junk mail at bay.

As a result the junk mail folder tends to pile up with never-to-be-read emails.

But, occasionally, an important email is snagged by the filter and is unduly ignored.

We can think of the human genome as a server sending out a constant bombardment of emails. These messages are on average 2,000 letters long, and these “letters” are made up of different types of bases, some of which are packaged in the form of RNA.

A new study has created a cause-and-effect link between chronic high blood sugar and disruption of mitochondria, the energy factories that create the metabolic energy that power most of our cells. 

Previous experiments by other research groups had shown that the high blood sugar of untreated diabetes alters the activity of mitochondria, compartments that process nutrients into useable energy for cells. To find out why, postdoctoral fellow Dr. Partha Banerjee compared the enzymes in mitochondria from the hearts of rats with diabetes to those from healthy rat hearts. He looked for differences in levels of two enzymes that add and remove a molecule called O-GlcNAc to proteins.  

To understand how transposable elements, DNA sequences capable of moving independently,  shape genomes, where they are maintained over generations, it is vital to discover the mechanisms behind their targeted integration.

Researchers from the Laboratoire Pathologie et Virologie Moléculaire (CNRS/Inserm/Université Paris Diderot), Institut de biologie intégrative de la cellule and the University of Minnesota have identified an interaction between two proteins that is essential for the integration of a transposable element into a specific area of the yeast genome. The results emphasize the role of these mobile DNA sequences in the evolution and adaptation of organisms, and their potential value for gene therapy.