ATP-binding cassette transporters are required for efficient RNA interference in Caenorhabditis elegans

被引:33
作者
Sundaram, Prema [1 ]
Echalier, Benjamin [1 ]
Han, Wang [1 ]
Hull, Dawn [1 ]
Timmons, Lisa [1 ]
机构
[1] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
关键词
GERM-LINE DEVELOPMENT; DOUBLE-STRANDED-RNA; CLASS-II REGION; C-ELEGANS; MULTIDRUG-RESISTANCE; GENETIC INTERFERENCE; ABC TRANSPORTERS; P-GLYCOPROTEIN; HELICASE; DCR-1;
D O I
10.1091/mbc.E06-03-0192
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RNA interference (RNAi) is a conserved gene-silencing phenomenon that can be triggered by delivery of double-stranded RNA (dsRNA) to cells and is a widely exploited technology in analyses of gene function. Although a number of proteins that facilitate RNAi have been identified, current descriptions of RNAi and interrelated mechanisms are far from complete. Here, we report that the Caenorhabditis elegans gene haf-6 is required for efficient RNAi. HAF-6 is a member of the ATP-binding cassette (ABC) transporter gene superfamily. ABC transporters use ATP to translocate small molecule substrates across the membranes in which they reside, often against a steep concentration gradient. Collectively, ABC transporters are involved in a variety of activities, including protective or barrier mechanisms that export drugs or toxins from cells, organellar biogenesis, and mechanisms that protect against viral infection. HAF-6 is expressed predominantly in the intestine and germline and is localized to intracellular reticular organelles. We further demonstrate that eight additional ABC genes from diverse subfamilies are each required for efficient RNAi in C. elegans. Thus, the ability to mount a robust RNAi response to dsRNA depends upon the deployment of two ancient systems that respond to environmental assaults: RNAi mechanisms and membrane transport systems that use ABC proteins.
引用
收藏
页码:3678 / 3688
页数:11
相关论文
共 70 条
[1]   The ABCs of immunology:: Structure and function of TAP, the transporter associated with antigen processing [J].
Abele, R ;
Tampé, R .
PHYSIOLOGY, 2004, 19 :216-224
[2]   Characterization of the human ABC superfamily: Isolation and mapping of 21 new genes using the expressed sequence tags database [J].
Allikmets, R ;
Gerrard, B ;
Hutchinson, A ;
Dean, M .
HUMAN MOLECULAR GENETICS, 1996, 5 (10) :1649-1655
[3]   SMG-5, required for C-elegans nonsense-mediated mRNA decay, associates with SMG-2 and protein phosphatase 2A [J].
Anders, KR ;
Grimson, A ;
Anderson, P .
EMBO JOURNAL, 2003, 22 (03) :641-650
[4]   ADRENOLEUKODYSTROPHY AND OTHER PEROXISOMAL DISEASES [J].
AUBOURG, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (03) :407-411
[5]   Inventory and function of yeast ABC proteins: about sex, stress, pleiotropic drug and heavy metal resistance [J].
Bauer, BE ;
Wolfger, H ;
Kuchler, K .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1461 (02) :217-236
[6]   ABC transporters and the blood-brain barrier [J].
Begley, DJ .
CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (12) :1295-1312
[7]   RNA meets chromatin [J].
Bernstein, E ;
Allis, CD .
GENES & DEVELOPMENT, 2005, 19 (14) :1635-1655
[8]  
BRENNER S, 1974, GENETICS, V77, P71
[9]   Homologues of the human multidrug resistance genes MRP and MDR contribute to heavy metal resistance in the soil nematode Caenorhabditis elegans [J].
Broeks, A ;
Gerrard, B ;
Allikmets, R ;
Dean, M ;
Plasterk, RHA .
EMBO JOURNAL, 1996, 15 (22) :6132-6143
[10]   A micrococcal nuclease homologue in RNAi effector complexes [J].
Caudy, AA ;
Ketting, RF ;
Hammond, SM ;
Denli, AM ;
Bathoorn, AMP ;
Tops, BBJ ;
Silva, JM ;
Myers, MM ;
Hannon, GJ ;
Plasterk, RHA .
NATURE, 2003, 425 (6956) :411-414