Summary: Scientists have identified how the brain protein cypin helps maintain strong connections between neurons, a discovery with implications for treating brain injuries and neurodegenerative diseases. Cypin ensures proper protein tagging at synapses, allowing neurons to communicate effectively and support memory and learning.
The research also revealed cypin slows protein breakdown and boosts synaptic proteins, enhancing brain cell signaling. These findings highlight cypin as a promising target for therapies aimed at restoring healthy brain function.
Key Facts:
- Cypin helps tag and position proteins at synapses, strengthening neuron communication.
- It interacts with protein breakdown systems to increase essential synaptic proteins.
- Enhancing cypin could improve memory and counteract neurodegenerative diseases and brain injury.
Source: Rutgers University
Scientists have discovered how a key protein helps maintain strong connections between brain cells that are crucial for learning and memory.
Results of the study, published in the journal Science Advances, could point the way to new treatments for traumatic brain injuries and diseases, such as Parkinson’s and Alzheimer’s, the scientists said.
Their research, led by a Rutgers University-New Brunswick professor, uncovered a previously unknown role for cypin, a brain protein. Members of the research team found that cypin promotes the presence of tags on specific proteins at synapses, namely the tiny gaps where the brain cells, known as neurons, communicate.
The marking helps ensure that the right proteins are in the right place, allowing the synapses to work properly.
The researchers said the insight has potentially profound implications for the treatment of brain disorders.
“Our research indicates that developing treatments or therapies that specifically focus on the protein cypin may help improve the connections between brain cells, enhancing memory and thinking abilities,” said Bonnie Firestein, a Distinguished Professor in the Department of Cell Biology and Neuroscience in the School of Arts and Sciences and an author of the study.
“These findings suggest that cypin could be used to develop treatments for neurodegenerative and neurocognitive diseases, as well as brain injuries.”
Firestein has been studying cypin for more than two decades. Her latest work uncovered several important aspects of how cypin functions and why it is significant for brain health.
One of the crucial discoveries is that cypin helps add a special tag to proteins in synapses connecting neurons. This tag ensures proteins are correctly positioned and able to send signals effectively. Proper tagging and movement of proteins are essential for the neurons to function correctly.
Another important finding is that cypin interacts with a complex of proteins, known as the proteasome, which is responsible for breaking down proteins. When cypin attaches or binds to the proteasome, it slows down this breakdown process, leading to an accumulation of proteins. This buildup can positively affect various cellular functions, which are important for the communication between neurons.
Firestein’s research also shows that when there is more cypin present, the levels of important proteins in the synapses increase. These proteins are vital for effective communication between neurons, empowering learning and memory.
Additionally, cypin increases the activity of another protein called UBE4A, which also helps with the tagging process. This indicates that cypin’s influence on synaptic proteins is partly because of its effect on UBE4A.
The work highlights the importance of cypin in maintaining healthy brain function and its potential as a target for therapeutic interventions.
“Even though this study is what we call ‘basic research,’ it eventually can be applied in practical, clinical settings,” said Firestein, who already is conducting such “translational” work in parallel.
Translational research is a type of research that takes discoveries made in the lab and turns them into practical treatments or solutions to improve human health.
Cypin’s significant role in the workings of the brain’s synapses makes it highly relevant to the potential treatment of neurodegenerative diseases and traumatic brain injury, she said. For example, healthy synaptic function is often disrupted in diseases such as Alzheimer’s and Parkinson’s.
In addition, the protein’s role in promoting synaptic plasticity – the ability of synapses to strengthen or weaken over time – means it may be used to help counteract the synaptic dysfunction seen in neurodegenerative diseases and brain injuries.
Funding: The study was supported in part by the National Institutes of Health (NINDS), the Coalition for Brain Injury Research, a charitable foundation dedicated to the memory of Dennis John Benigno, who suffered a traumatic brain injury in junior high school; and private donors Jamuna Rajasingham and Dyan Rajasingham.
Other scientists from Rutgers involved in the study include Kiran Madura, a professor in the Department of Pharmacology at Robert Wood Johnson Medical School; Srinivasa Gandu, Mihir Patel, Ana Rodriguez, former doctoral students in the Department of Cell Biology and Neuroscience.
Jared Lamp and Irving Vega of Michigan State University also contributed to this research.
About this genetics and memory research news
Author: Kitta MacPherson
Source: Rutgers University
Contact: Kitta MacPherson – Rutgers University
Image: The image is credited to Neuroscience News
Original Research: Open access.
“Cypin regulates K63-linked polyubiquitination to shape synaptic content” by Bonnie Firestein et al. Science Advances
Abstract
Cypin regulates K63-linked polyubiquitination to shape synaptic content
An open question in neuroscience is how protein posttranslational modifications regulate synaptic site targeting.
Polyubiquitination plays a role in proteasome-mediated protein turnover; however, additional functions for specific types of polyubiquitin linkages have been identified.
One type of polyubiquitination, K63-polyubiquitin (K63-polyUb), has been studied for its role in signal transduction within the context of cancer, but little has been done to uncover its role regarding neuronal and synaptic function.
Here, we report an emerging function for the cytosolic PSD-95 interactor, cypin, in the regulation of synaptic content by K63-polyUb during neuronal development in vitro and in adult mice in vivo.
We identify cypin-promoted K63-polyUb on postsynaptic proteins and also find an important role for cypin in presynaptic function.
Our work demonstrates that cypin-promoted changes to K63-polyUb can regulate synaptic content and function on both sides of the synapse, adding important insight into basic mechanisms of neuronal signaling.