小鼠肾近曲小管的昼夜节律基因表达

IF 3.7 2区 医学 Q1 PHYSIOLOGY American Journal of Physiology-renal Physiology Pub Date : 2023-03-01 Epub Date: 2023-02-02 DOI:10.1152/ajprenal.00231.2022
Molly A Bingham, Kim Neijman, Chin-Rang Yang, Angel Aponte, Angela Mak, Hiroaki Kikuchi, Hyun Jun Jung, Brian G Poll, Viswanathan Raghuram, Euijung Park, Chung-Lin Chou, Lihe Chen, Jens Leipziger, Mark A Knepper, Margo Dona
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引用次数: 0

摘要

肾脏功能的昼夜节律变化已被广泛认可,但在生理实验中却往往被忽视,成为一个潜在的干扰变量。在这里,我们创建了一个数据资源,其中包括小鼠近端小管微切片中 mRNA 转录物的表达水平与一天中时间的函数关系。小样本 RNA 测序适用于显微解剖的 S1 近端曲小管和 S2 近端直小管。经过严格过滤后,使用 JTK-Cycle 对数据进行分析,以检测周期性。该数据集以用户友好型网页的形式提供,网址为 https://esbl.nhlbi.nih.gov/Databases/Circadian-Prox2/。在近端曲小管中,234 个转录本以昼夜节律的方式变化(占总数的 4.0%)。在近端直小管中,334 个转录本以昼夜节律方式变化(占总数的 5.3%)。研究发现,以前已知的与皮质类固醇作用和血流量增加有关的转录本在昼夜节律转录本中所占比例过高,这些转录本在一天中的 "黑暗 "时段[ZT(Zeitgeber time)14-22]达到峰值,与小鼠皮质类固醇和肾小球滤过率的峰值水平相对应。为了探究肾脏中的蛋白质丰度是否与时间相关,我们在 ZT12 和 ZT0 时对小鼠全肾进行了基于 LC-MS/MS 的蛋白质组学研究。完整的数据集(n = 6,546 个蛋白质)可在 https://esbl.nhlbi.nih.gov/Databases/Circadian-Proteome/ 上获得。总体而言,有 293 个蛋白质在 ZT12 和 ZT0 之间有差异表达(197 个蛋白质在 ZT12 表达量更高,96 个蛋白质在 ZT0 表达量更高)。在受调控的蛋白质中,只有 9 个蛋白质在 RNA 序列分析中是周期性的,这表明蛋白质丰度受到转录后的高度调控。作者利用RNA测序转录组学和基于LC-MS/MS的蛋白质组学确定了以周期性方式表达的基因产物。这些数据被用来构建用户友好型网络资源。
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Circadian gene expression in mouse renal proximal tubule.

Circadian variability in kidney function is well recognized but is often ignored as a potential confounding variable in physiological experiments. Here, we have created a data resource consisting of expression levels for mRNA transcripts in microdissected proximal tubule segments from mice as a function of the time of day. Small-sample RNA sequencing was applied to microdissected S1 proximal convoluted tubules and S2 proximal straight tubules. After stringent filtering, the data were analyzed using JTK-Cycle to detect periodicity. The data set is provided as a user-friendly webpage at https://esbl.nhlbi.nih.gov/Databases/Circadian-Prox2/. In proximal convoluted tubules, 234 transcripts varied in a circadian manner (4.0% of the total). In proximal straight tubules, 334 transcripts varied in a circadian manner (5.3%). Transcripts previously known to be associated with corticosteroid action and with increased flow were found to be overrepresented among circadian transcripts peaking during the "dark" portion of the day [zeitgeber time (ZT)14-22], corresponding to peak levels of corticosterone and glomerular filtration rate in mice. To ask whether there is a time-of-day dependence of protein abundances in the kidney, we carried out LC-MS/MS-based proteomics in whole mouse kidneys at ZT12 and ZT0. The full data set (n = 6,546 proteins) is available at https://esbl.nhlbi.nih.gov/Databases/Circadian-Proteome/. Overall, 293 proteins were differentially expressed between ZT12 and ZT0 (197 proteins greater at ZT12 and 96 proteins greater at ZT0). Among the regulated proteins, only nine proteins were found to be periodic in the RNA-sequencing analysis, suggesting a high level of posttranscriptional regulation of protein abundances.NEW & NOTEWORTHY Circadian variation in gene expression can be an important determinant in the regulation of kidney function. The authors used RNA-sequencing transcriptomics and LC-MS/MS-based proteomics to identify gene products expressed in a periodic manner. The data were used to construct user-friendly web resources.

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来源期刊
CiteScore
8.40
自引率
7.10%
发文量
154
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology - Renal Physiology publishes original manuscripts on timely topics in both basic science and clinical research. Published articles address a broad range of subjects relating to the kidney and urinary tract, and may involve human or animal models, individual cell types, and isolated membrane systems. Also covered are the pathophysiological basis of renal disease processes, regulation of body fluids, and clinical research that provides mechanistic insights. Studies of renal function may be conducted using a wide range of approaches, such as biochemistry, immunology, genetics, mathematical modeling, molecular biology, as well as physiological and clinical methodologies.
期刊最新文献
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