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转录组分析揭示快速眼动睡眠剥夺大鼠大脑中与记忆和神经传递相关基因的表达变化。

Transcriptome Analysis Reveals Altered Expression of Memory and Neurotransmission Associated Genes in the REM Sleep Deprived Rat Brain.

作者信息

Narwade Santosh C, Mallick Birendra N, Deobagkar Deepti D

机构信息

Molecular Biology Research Laboratory, Center of Advanced Studies, Department of Zoology, Savitribai Phule Pune University Pune, India.

School of Life Sciences, Jawaharlal Nehru University New Delhi, India.

出版信息

Front Mol Neurosci. 2017 Mar 17;10:67. doi: 10.3389/fnmol.2017.00067. eCollection 2017.

DOI:10.3389/fnmol.2017.00067
PMID:28367113
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5355427/
Abstract

Sleep disorders are associated with cognitive impairment. Selective rapid eye movement sleep (REMS) deprivation (REMSD) alters several physiological processes and behaviors. By employing NGS platform we carried out transcriptomic analysis in brain samples of control rats and those exposed to REMSD. The expression of genes involved in chromatin assembly, methylation, learning, memory, regulation of synaptic transmission, neuronal plasticity and neurohypophysial hormone synthesis were altered. Increased transcription of BMP4, DBH and ATP1B2 genes after REMSD supports our earlier findings and hypothesis. Alteration in the transcripts encoding histone subtypes and important players in chromatin remodeling was observed. The mRNAs which transcribe neurotransmitters such as OXT, AVP, PMCH and LNPEP and two small non-coding RNAs, namely RMRP and BC1 were down regulated. At least some of these changes are likely to regulate REMS and may participate in the consequences of REMS loss. Thus, the findings of this study have identified key epigenetic regulators and neuronal plasticity genes associated to REMS and its loss. This analysis provides a background and opens up avenues for unraveling their specific roles in the complex behavioral network particularly in relation to sustained REMS-loss associated changes.

摘要

睡眠障碍与认知障碍有关。选择性快速眼动睡眠(REMS)剥夺(REMSD)会改变多种生理过程和行为。通过使用NGS平台,我们对对照大鼠和暴露于REMSD的大鼠的脑样本进行了转录组分析。参与染色质组装、甲基化、学习、记忆、突触传递调节、神经元可塑性和神经垂体激素合成的基因表达发生了改变。REMSD后BMP4、DBH和ATP1B2基因转录增加,支持了我们早期的发现和假设。观察到编码组蛋白亚型和染色质重塑重要参与者的转录本发生了改变。转录神经递质如OXT、AVP、PMCH和LNPEP的mRNA以及两个小非编码RNA,即RMRP和BC1被下调。这些变化中至少有一些可能调节快速眼动睡眠,并可能参与快速眼动睡眠丧失的后果。因此,本研究的结果确定了与快速眼动睡眠及其丧失相关的关键表观遗传调节因子和神经元可塑性基因。该分析提供了一个背景,并为揭示它们在复杂行为网络中的特定作用开辟了途径,特别是与持续快速眼动睡眠丧失相关的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/36658affb912/fnmol-10-00067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/8d5f0b9ba940/fnmol-10-00067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/65953922571d/fnmol-10-00067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/2a61c78e4104/fnmol-10-00067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/4717b870754c/fnmol-10-00067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/36658affb912/fnmol-10-00067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/8d5f0b9ba940/fnmol-10-00067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/65953922571d/fnmol-10-00067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/2a61c78e4104/fnmol-10-00067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/4717b870754c/fnmol-10-00067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aaf/5355427/36658affb912/fnmol-10-00067-g005.jpg

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