“We know that defects in beta cells can lead to high levels of glucose in the blood and, eventually, diabetes.” said Dr. Dina Mostafa, former PhD student in the Unit and first author of the paper published in Communications Biology. “Our results suggest that CNOT3 has a hand in this and plays a key role in maintaining normal beta cell function.”
Knocking out CNOT3 found to lead to diabetes in mice
CNOT3 is a jack-of-all-trades. Many organs throughout the body express it, and it regulates different genes in different tissues. But its activity has a common basis – it helps to keep cells alive, healthy, and functioning correctly. It does this through several different mechanisms, such as producing the right proteins or suppressing certain genes.Here, researchers studied its function in islet cells from pancreatic tissue in mice. These islets are notoriously difficult to work with, taking up just only one to two percent of the pancreas, but they’re where the beta cells are located.
The researchers first looked at whether CNOT3 expression differed in diabetic mice compared with non-diabetic mice. By looking at these islets, they found that there was a significant decrease in the CNOT3 in the diabetic islets as opposed to the non-diabetic ones.
To further investigate the protein’s function, the researchers blocked its production in the beta cells of otherwise normal mice. For four weeks, the animals’ metabolism functioned normally, but by the eighth week, they had developed an intolerance to glucose, and by 12 weeks they had full-blown diabetes.
Mice lacking CNOT3 in pancreatic beta cells have fewer insulin-producing cells, leading to diabetes.
Without CNOT3, the researchers found that some genes, which are normally switched off in beta cells, switch on and start to produce proteins. Under normal circumstances, these genes are silenced because once they switch on, they cause all kinds of problems for the beta cells, such as stopping them from secreting insulin in response to glucose.“We still don’t know that much about these kinds of genes, such as what their normal function is and the mechanism that’s involved in their silencing,” Dr. Mostafa said. “So, it was very rewarding to find that CNOT3 in an important factor in keeping them switched off.”
The messenger RNA connection
Further research into the cellular mechanisms behind this found a surprising link between CNOT3 and the messenger RNA of these normally switched-off genes. A messenger RNA (mRNA) is a single strand molecule that corresponds to the genetic sequence of a gene and is essential for synthesizing proteins.Under normal circumstances, the mRNA of these genes hardly expresses. But once CNOT3 was removed, the researchers found that the mRNA was much more stable. In fact, protein was produced from the stabilized mRNA, which have unfavorable effects on normal tissue function. This suggests that at least one way that these genes are kept switch off is through the destabilization of their mRNA, driven by CNOT3.
“This study is a step towards understanding the molecular mechanisms that govern normal beta cell function,” Dr. Mostafa said. “Ultimately, it could contribute to new ways of preventing and treating diabetes.”
The researchers from the Cell Signal Unit at OIST. From left, Dr. Akiko Yanagiya, Dr. Dina Mostafa, and Professor Tadashi Yamamoto.
Alongside Dr. Mostafa, the research group included Dr. Akiko Yanagiya and Professor Tadashi Yamamoto from OIST’s Cell Signal Unit, Dr. Eleni Georgiadou and Professor Guy A. Rutter from Imperial College London, Dr. Yibo Wu and Dr. Toru Suzuki from Riken Center of Integrative Medical Sciences, and Dr. Theodoros Stylianides from Loughborough University.By Lucy Dickie
oist.jp
