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
[31]   Systematic functional analysis of the Caenorhabditis elegans genome using RNAi [J].
Kamath, RS ;
Fraser, AG ;
Dong, Y ;
Poulin, G ;
Durbin, R ;
Gotta, M ;
Kanapin, A ;
Le Bot, N ;
Moreno, S ;
Sohrmann, M ;
Welchman, DP ;
Zipperlen, P ;
Ahringer, J .
NATURE, 2003, 421 (6920) :231-237
[32]  
Kelly WG, 1997, GENETICS, V146, P227
[33]   A conserved siRNA-degrading RNase negatively regulates RNA interference in C-elegans [J].
Kennedy, S ;
Wang, D ;
Ruvkun, G .
NATURE, 2004, 427 (6975) :645-649
[34]   mut-7 of C-elegans, required for transposon silencing and RNA interference, is a homolog of Werner syndrome helicase and RNaseD [J].
Ketting, RF ;
Haverkamp, THA ;
van Luenen, HGAM ;
Plasterk, RHA .
CELL, 1999, 99 (02) :133-141
[35]  
Kim JK, 2005, SCIENCE, V308, P1164, DOI 10.1126/science.1109267
[36]   A role for the RNase III enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans [J].
Knight, SW ;
Bass, BL .
SCIENCE, 2001, 293 (5538) :2269-2271
[37]   Predicting transmembrane protein topology with a hidden Markov model: Application to complete genomes [J].
Krogh, A ;
Larsson, B ;
von Heijne, G ;
Sonnhammer, ELL .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 305 (03) :567-580
[38]   Interacting endogenous and exogenous RNAi pathways in Caenorhabditis elegans [J].
Lee, RC ;
Hammell, CM ;
Ambros, V .
RNA, 2006, 12 (04) :589-597
[39]   Antiviral silencing in animals [J].
Li, HW ;
Ding, SW .
FEBS LETTERS, 2005, 579 (26) :5965-5973
[40]   MTABC3, a novel mitochondrial ATP-binding cassette protein involved in iron homeostasis [J].
Mitsuhashi, N ;
Miki, T ;
Senbongi, H ;
Yokoi, N ;
Yano, H ;
Miyazaki, M ;
Nakajima, N ;
Iwanaga, T ;
Yokoyama, Y ;
Shibata, T ;
Seino, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17536-17540