Whole Genome RNAi Screen in C. elegans Identifies CAB-1 as a Novel Regulator of DCV Secretion

被引:1
|
作者
Xia Zhi-Ping [1 ,3 ]
Chen Yan [1 ,3 ]
Sheng Yi [1 ,2 ]
Yi Ya-Lan [1 ,3 ]
Song E-Li [1 ]
Xu Tao [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing 100101, Peoples R China
[2] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Wuhan 430074, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
CAB-1; defecation; dense core vesicle (DCV); secretion; whole genome RNAi screen; DENSE-CORE VESICLE; CAENORHABDITIS-ELEGANS; GENETIC INTERFERENCE; HOMOTYPIC FUSION; MATURATION; RELEASE; NEURONS; ACIDIFICATION; NEUROPEPTIDE; EXOCYTOSIS;
D O I
10.3724/SP.J.1206.2014.00047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The dense core vesicle (DCV) is a key organelle involved in the secretion of hormones and neuropeptides in endocrine cells and neurons in response to stimulation. However, the mechanisms underlying its biogenesis, trafficking and exocytosis remain largely unknown. In this study, to discover novel players functioning in DCV secretion, we performed a genome-wide RNAi screen in C. elegans by observing worm defecation behavior. A series of genes that function in the intestine to regulate DCV biogenesis or exocytosis were successfully identified, including CAB-1, which was further determined to be a specific regulator for DCV exocytosis. In the intestine, cab-1 mutation causes reduced secretion of intestinal DCV cargoes. In the nervous system, the loss of CAB-1 leads to the accumulation of DCV markers in the presynaptic region, but synaptic vesicles are not affected. This work demonstrates that CAB-1 is a regulatory factor specifically involved in DCV secretion.
引用
收藏
页码:787 / 795
页数:9
相关论文
共 48 条
  • [1] Bonnemaison Mathilde L, 2013, Front Endocrinol (Lausanne), V4, P101, DOI 10.3389/fendo.2013.00101
  • [2] BRENNER S, 1974, GENETICS, V77, P71
  • [3] Secretory granule exocytosis
    Burgoyne, RD
    Morgan, A
    [J]. PHYSIOLOGICAL REVIEWS, 2003, 83 (02) : 581 - 632
  • [4] Regulation of retrograde signaling at neuromuscular junctions by the novel C2 domain protein AEX-1
    Doi, M
    Iwasaki, K
    [J]. NEURON, 2002, 33 (02) : 249 - 259
  • [5] Impaired dense core vesicle maturation in Caenorhabditis elegans mutants lacking Rab2
    Edwards, Stacey L.
    Charlie, Nicole K.
    Richmond, Janet E.
    Hegermann, Jan
    Eimer, Stefan
    Miller, Kenneth G.
    [J]. JOURNAL OF CELL BIOLOGY, 2009, 186 (06): : 881 - 895
  • [6] Oscillatory Ca2+ signaling in the isolated Caenorhabditis elegans intestine:: Role of the inositol-1,4,5-trisphosphate receptor and phospholipases C β and γ
    Espelt, MV
    Estevez, AY
    Yin, XY
    Strange, K
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2005, 126 (04): : 379 - 392
  • [7] Evans T., 2006, TRANSFORMATION MICRO
  • [8] RAB-27 and its effector RBF-1 regulate the tethering and docking steps of DCV exocytosis in C. elegans
    Feng WanJuan
    Liang Tao
    Yu JunWei
    Zhou Wei
    Zhang YongDeng
    Wu ZhengXing
    Xu Tao
    [J]. SCIENCE CHINA-LIFE SCIENCES, 2012, 55 (03) : 228 - 235
  • [9] Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans
    Fire, A
    Xu, SQ
    Montgomery, MK
    Kostas, SA
    Driver, SE
    Mello, CC
    [J]. NATURE, 1998, 391 (6669) : 806 - 811
  • [10] AP-1 recruitment to VAMP4 is modulated by phosphorylation-dependent binding of PACS-1
    Hinners, I
    Wendler, F
    Fei, H
    Thomas, L
    Thomas, G
    Tooze, SA
    [J]. EMBO REPORTS, 2003, 4 (12) : 1182 - 1189