The 5′-3′ exoribonuclease pacman is required for epithelial sheet sealing in Drosophila and genetically interacts with the phosphatase puckered

被引:20
作者
Grima, Dominic P. [1 ]
Sullivan, Melanie [1 ]
Zabolotskaya, Maria V. [1 ]
Browne, Cathy [2 ]
Seago, Julian [3 ]
Wan, Kay Chong [2 ]
Okada, Yoshio [4 ]
Newbury, Sarah F. [1 ]
机构
[1] Univ Sussex, Brighton & Sussex Med Sch, Brighton BN1 9PS, E Sussex, England
[2] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[3] Inst Anim Hlth, Pirbright GU24 0NF, Surrey, England
[4] Bio21 Corp, Okinawa 901242, Japan
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1042/BC20080049
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background information. Ribonucleases have been well studied in yeast and bacteria, but their biological significance to developmental processes in multicellular organisms is not well understood. However, there is increasing evidence that specific timed transcript degradation is critical for regulation of many cellular processes, including translational repression, nonsense-mediated decay and RNA interference. The Drosophila gene pacman is highly homologous to the major yeast exoribonuclease XRN1 and is the only known cytoplasmic 5'-3' exoribonuclease in eukaryotes. To determine the effects of this exoribonuclease in development we have constructed a number of mutations in pacman by P-element excision and characterized the resulting phenotypes. Results. Mutations in pacman resulted in flies with a number of specific phenotypes, such as low viability, dull wings, crooked legs, failure of correct dorsal/thorax closure and defects in wound healing. The epithelial sheet movement involved in dorsal/thorax closure is a conserved morphogenetic process which is similar to that of hind-brain closure in vertebrates and wound healing in humans. As the JNK (c-Jun N-terminal kinase) signalling pathway is known to be involved in dorsal/thorax closure and wound healing, we tested whether pacman affects JNK signalling. Our experiments demonstrate that pacman genetically interacts with puckered, a phosphatase that negatively regulates the JNK signalling pathway. Conclusions. These results reveal that the 5'-3' exoribonuclease pacman is required for a critical aspect of epithelial sheet sealing in Drosophila. Since these mutations result in specific phenotypes, our data suggest that the exoribonuclease Pacman targets a specific subset of mRNAs involved in this process. One of these targets could be a member of the JNK signalling pathway, although it is possible that a parallel pathway may instead be affected. The exoribonuclease pacman is highly conserved in all eukaryotes, therefore it is likely that it is involved in similar morphological processes, such as wound healing in human cells.
引用
收藏
页码:687 / 701
页数:15
相关论文
共 60 条
[1]  
Agnès F, 1999, DEVELOPMENT, V126, P5453
[2]   The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex [J].
Anderson, JSJ ;
Parker, R .
EMBO JOURNAL, 1998, 17 (05) :1497-1506
[3]  
[Anonymous], 1989, Molecular Cloning
[4]   Staufen- and FMRP-containing neuronal RNPs are structurally and functionally related to somatic P bodies [J].
Barbee, Scott A. ;
Estes, Patricia S. ;
Cziko, Anne-Marie ;
Hillebrand, Jens ;
Luedeman, Rene A. ;
Coller, Jeff M. ;
Johnson, Nick ;
Howlett, Iris C. ;
Geng, Cuiyun ;
Ueda, Ryu ;
Brand, Andrea H. ;
Newbury, Sarah F. ;
Wilhelm, James E. ;
Levine, Richard B. ;
Nakamura, Akira ;
Parker, Roy ;
Ramaswami, Mani .
NEURON, 2006, 52 (06) :997-1009
[5]   Spatial and temporal control of RNA stability [J].
Bashirullah, A ;
Cooperstock, RL ;
Lipshitz, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (13) :7025-7028
[6]   A mouse cytoplasmic exoribonuclease (mXRN1p) with preference for G4 tetraplex substrates [J].
Bashkirov, VI ;
Scherthan, H ;
Solinger, JA ;
Buerstedde, JM ;
Heyer, WD .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :761-773
[7]   A Sm-like protein complex that participates in mRNA degradation [J].
Bouveret, E ;
Rigaut, G ;
Shevchenko, A ;
Wilm, M ;
Séraphin, B .
EMBO JOURNAL, 2000, 19 (07) :1661-1671
[8]   Integrins as mediators of morphogenesis in Drosophila [J].
Brown, NH ;
Gregory, SL ;
Martin-Bermudo, ZD .
DEVELOPMENTAL BIOLOGY, 2000, 223 (01) :1-16
[9]   Mechanisms and control of mRNA turnover in Saccharomyces cerevisiae [J].
Caponigro, G ;
Parker, R .
MICROBIOLOGICAL REVIEWS, 1996, 60 (01) :233-+
[10]   Regulation of Rho and Rac signaling to the actin cyloskeleton by paxillin during Drosophila development [J].
Chen, GC ;
Turano, B ;
Ruest, PJ ;
Hagel, M ;
Settleman, J ;
Thomas, SA .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (03) :979-987