Hox Proteins Mediate Developmental and Environmental Control of Autophagy

被引:43
作者
Banreti, Agnes [1 ,2 ]
Hudry, Bruno [1 ]
Sass, Miklos [2 ]
Saurin, Andrew J. [1 ]
Graba, Yacine [1 ]
机构
[1] Aix Marseille Univ, CNRS, IBDML, UMR 7288, F-13288 Marseille 09, France
[2] Eotvos Lorand Univ, Dept Anat Cell & Dev Biol, H-1117 Budapest, Hungary
关键词
FAT-BODY; POSSIBLE INVOLVEMENT; BITHORAX COMPLEX; AMINO-ACID; DROSOPHILA; GENES; MAINTENANCE; HOMEOSTASIS; EXPRESSION; ECDYSONE;
D O I
10.1016/j.devcel.2013.11.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hox genes encode evolutionarily conserved transcription factors, providing positional information used for differential morphogenesis along the anteroposterior axis. Here, we show that Drosophila Hox proteins are potent repressors of the autophagic process. In inhibiting autophagy, Hox proteins display no apparent paralog specificity and do not provide positional information. Instead, they impose temporality on developmental autophagy and act as effectors of environmental signals in starvation-induced autophagy. Further characterization establishes that temporality is controlled by Pontin, a facultative component of the Brahma chromatin remodeling complex, and that Hox proteins impact on autophagy by repressing the expression of core components of the autophagy machinery. Finally, the potential of central and posterior mouse Hox proteins to inhibit autophagy in Drosophila and in vertebrate COS-7 cells indicates that regulation of autophagy is an evolutionary conserved feature of Hox proteins.
引用
收藏
页码:56 / 69
页数:14
相关论文
共 43 条
[1]   The Drosophila BRM complex facilitates global transcription by RNA polymerase II [J].
Armstrong, JA ;
Papoulas, O ;
Daubresse, G ;
Sperling, AS ;
Lis, JT ;
Scott, MP ;
Tamkun, JW .
EMBO JOURNAL, 2002, 21 (19) :5245-5254
[2]   How death shapes life during development [J].
Baehrecke, EH .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (10) :779-787
[3]  
Beck S, 2010, ADV EXP MED BIOL, V689, P41
[4]   Autophagy and cell death: No longer at odds [J].
Bergmann, Andreas .
CELL, 2007, 131 (06) :1032-1034
[5]   DOUBLE AND TRIPLE MUTANT COMBINATIONS OF THE BITHORAX COMPLEX OF DROSOPHILA [J].
CASANOVA, J ;
SANCHEZHERRERO, E ;
BUSTURIA, A ;
MORATA, G .
EMBO JOURNAL, 1987, 6 (10) :3103-3109
[6]  
CASTELLIGAIR J, 1994, DEVELOPMENT, V120, P1983
[7]   Genome-Wide Analysis of the Binding of the Hox Protein Ultrabithorax and the Hox Cofactor Homothorax in Drosophila [J].
Choo, Siew Woh ;
White, Robert ;
Russell, Steven .
PLOS ONE, 2011, 6 (04)
[8]   TOR kinase homologs function in a signal transduction pathway that is conserved from yeast to mammals [J].
Cutler, NS ;
Heitman, J ;
Cardenas, ME .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 155 (1-2) :135-142
[9]   A simple and efficient method to identify replacements of P-lacZ by P-Gal4 lines allows obtaining Gal4 insertions in the bithorax complex of Drosophila [J].
de Navas, Luis ;
Foronda, David ;
Suzanne, Magali ;
Sanchez-Herrero, Ernesto .
MECHANISMS OF DEVELOPMENT, 2006, 123 (11) :860-867
[10]   Reptin and Pontin function antagonistically with PcG and TrxG complexes to mediate Hox gene control [J].
Diop, Soda Balla ;
Bertaux, Karine ;
Vasanthi, Dasari ;
Sarkeshik, Ali ;
Goirand, Benjamin ;
Aragnol, Denise ;
Tolwinski, Nicholas S. ;
Cole, Michael D. ;
Pradel, Jacques ;
Yates, John R., III ;
Mishra, Rakesh K. ;
Graba, Yacine ;
Saurin, Andrew J. .
EMBO REPORTS, 2008, 9 (03) :260-266