RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides

被引:101
作者
Abruzzi, Katharine C.
Zadina, Abigail [2 ]
Luo, Weifei
Wiyanto, Evelyn [3 ]
Rahman, Reazur
Guo, Fang
Shafer, Orie [4 ]
Rosbash, Michael [1 ]
机构
[1] Brandeis Univ, Howard Hughes Med Inst, Waltham, MA 02254 USA
[2] Columbia Univ, Grad Sch Neurobiol & Behav, New York, NY USA
[3] Lake Erie Coll Osteopath Med, Erie, PA USA
[4] Univ Michigan, Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
来源
PLOS GENETICS | 2017年 / 13卷 / 02期
基金
美国国家科学基金会;
关键词
CIRCADIAN-RHYTHMS; GENE-EXPRESSION; SUPRACHIASMATIC NUCLEUS; NERVOUS-SYSTEM; NEUROMEDIN-U; OUTPUT; SLEEP; CRYPTOCHROME; ORGANIZATION; PEPTIDE;
D O I
10.1371/journal.pgen.1006613
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Locomotor activity rhythms are controlled by a network of similar to 150 circadian neurons within the adult Drosophila brain. They are subdivided based on their anatomical locations and properties. We profiled transcripts "around the clock" from three key groups of circadian neurons with different functions. We also profiled a non-circadian outgroup, dopaminergic (TH) neurons. They have cycling transcripts but fewer than clock neurons as well as low expression and poor cycling of clock gene transcripts. This suggests that TH neurons do not have a canonical circadian clock and that their gene expression cycling is driven by brain systemic cues. The three circadian groups are surprisingly diverse in their cycling transcripts and overall gene expression patterns, which include known and putative novel neuropeptides. Even the overall phase distributions of cycling transcripts are distinct, indicating that different regulatory principles govern transcript oscillations. This surprising cell-type diversity parallels the functional heterogeneity of the different neurons.
引用
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页数:23
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