Summary: The most common messenger RNA modification in mammals helps coordinate nerve cell response to memory inducting stimulus, a new study reveals.
Source: University of Chicago Medical Center.
RNA carries pieces of instructions encoded in DNA to coordinate the production of proteins that will carry out the work to be done in a cell. But the process isn’t always straightforward. Chemical modifications to DNA or RNA can alter the way genes are expressed without changing the actual genetic sequences. These epigenetic or epitranscriptome changes can affect many biological processes such as immune system response, nervous system development, various human cancers and even obesity.
Most of these changes happen through methylation, a process in which chemical molecules called methyl groups are added to a DNA or RNA molecule. Proteins that add a methyl group are known as “writers,” and proteins that can remove the methyl groups are “erasers.” For the methylation to have a biological effect, there must be “reader” proteins that can identify the change and bind to it.
The most common modification on messenger RNA in mammals is called N6-methyladenosine (m6A). It is widespread in the nervous system. It helps coordinate several neural functions, working through reader proteins in the YTH family of proteins.
In a new study published in Nature, scientists from the University of Chicago show how Ythdf1, a member of the YTH family that specifically recognizes m6A, plays an important role in the process of learning and memory formation. Using CRISPR/Cas9 gene editing tools to knock out Ythdf1in mice, they demonstrated how it promotes translation of m6A-modified messenger RNA (mRNA) in response to learning activities and direct nerve cell stimulus.
“This study opens the door to our future understanding of learning and memory,” said Chuan He, PhD, the John T. Wilson Distinguished Service Professor of Chemistry, Biochemistry and Molecular Biology at UChicago and one of the senior authors of the study. “We saw differences in long-term memory and learning between the normal and knockout mice, demonstrating that the m6A methylation plays a critical role through Ythdf1.”
In 2015, He published a study in Cell showing how Ythdf1 recognizes m6A-modified mRNAs and promotes their translation to proteins. The new study further demonstrates how this translation increases specifically in response to nervous system stimulation.
Hailing Shi, a graduate student in He’s lab, led the new study, working with colleagues from Shanghai Tech University in China and the University of Pennsylvania. Mice express more Ythdf1 mRNAs in the hippocampus, part of the brain crucial to spatial learning and memory. So, the researchers conducted several experiments with both normal mice and mice without Ythdf1 to test the effects on their ability to learn from experiences.
In one scenario called the Morris water maze to test spatial memory, they used a water tank with a submerged platform a mouse could stand on to avoid swimming. Mice got several tries to learn where the platforms were located based on visual cues in a testing room. Then the platform was removed. The normal mice did a better job remembering where the platform used to be than the knockout mice.
The researchers also tested contextual and auditory fear memory in the different groups of mice by administering electrical shocks in combination with certain sounds in specific settings. Again, the normal mice demonstrated better contextual memory than knockout mice. They showed a fear response after being placed in the same setting again without the associated sounds, but not after hearing the sounds in a different setting.
The memory and learning deficits were reversible, however. When the researchers injected knockout mice with a virus carrying Ythdf1, their performance on memory and learning tasks improved dramatically.
The researchers also tested the response of cultured mouse neurons directly in the lab. When the normal cells were stimulated, they increased new protein production, compared to much less activity in Ythdf1 knockout cells.
“It’s really an exciting finding to show how the protein can respond to a neuronal stimulus which could contribute to controlled translation,” Shi said.
“It’s a stimulation-dependent upregulation of translation,” He added. “It makes sense because you don’t want to fire up your neurons constantly, only when you have a stimulation.”
While the current study identifies one important function for YTHDF1, there may be many other functions involved with other biological processes.
“This is not just limited to learning and memory. This stimulation induced translation should apply to many other systems,” He said. “The same m6A modification is known to play a role in the immune system when there is an infection, or when a cell moves to a different part of the body. So, I think this is a general concept.”
Funding: Study supported by the National Institutes of Health, the National Key R&D Program of China, the National Natural Science Foundation of China, and the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation.
Additional authors include Xuliang Zhang, Zongyang Lu, Yajing Liu, Jianan Li, Piliang Hao, Yu Zhang, Xingxu Huang, and Tao Zhou from Shanghai Tech University, China; Yi-Lan Weng, Feng Zhang, Yijing Su, Guo-li Ming, and Hongjun Song from the University of Pennsylvania; Zhike Lu, Jary Y. Delgado, Meera J. Patel, Xiaoxi Zhuang from the University of Chicago; You Wu from Tongji University, China; Xiaohua Cao from East China Normal University; and Bin Shen from Nanjing Medical University, China.
Source: Matt Wood – University of Chicago Medical Center
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Abstract for “m6A facilitates hippocampus-dependent learning and memory through YTHDF1” by Hailing Shi, Xuliang Zhang, Yi-Lan Weng, Zongyang Lu, Yajing Liu, Zhike Lu, Jianan Li, Piliang Hao, Yu Zhang, Feng Zhang, You Wu, Jary Y. Delgado, Yijing Su, Meera J. Patel, Xiaohua Cao, Bin Shen, Xingxu Huang, Guo-li Ming, Xiaoxi Zhuang, Hongjun Song, Chuan He & Tao Zhou in Nature. Published October 31 2018.
m6A facilitates hippocampus-dependent learning and memory through YTHDF1
N6-methyladenosine (m6A), the most prevalent internal RNA modification on mammalian messenger RNAs, regulates the fates and functions of modified transcripts through m6A-specific binding proteins1,2,3,4,5. In the nervous system, m6A is abundant and modulates various neural functions6,7,8,9,10,11. Whereas m6A marks groups of mRNAs for coordinated degradation in various physiological processes12,13,14,15, the relevance of m6A for mRNA translation in vivo remains largely unknown. Here we show that, through its binding protein YTHDF1, m6A promotes protein translation of target transcripts in response to neuronal stimuli in the adult mouse hippocampus, thereby facilitating learning and memory. Mice with genetic deletion of Ythdf1 show learning and memory defects as well as impaired hippocampal synaptic transmission and long-term potentiation. Re-expression of YTHDF1 in the hippocampus of adult Ythdf1-knockout mice rescues the behavioural and synaptic defects, whereas hippocampus-specific acute knockdown of Ythdf1 or Mettl3, which encodes the catalytic component of the m6A methyltransferase complex, recapitulates the hippocampal deficiency. Transcriptome-wide mapping of YTHDF1-binding sites and m6A sites on hippocampal mRNAs identified key neuronal genes. Nascent protein labelling and tether reporter assays in hippocampal neurons showed that YTHDF1 enhances protein synthesis in a neuronal-stimulus-dependent manner. In summary, YTHDF1 facilitates translation of m6A-methylated neuronal mRNAs in response to neuronal stimulation, and this process contributes to learning and memory.