Positional cloning of a temperature-sensitive mutant emmental reveals a role for sly1 during cell proliferation in zebrafish fin regeneration

被引:50
作者
Nechiporuk, A [1 ]
Poss, KD
Johnson, SL
Keating, MT
机构
[1] Harvard Univ, Sch Med, Howard Hughes Med Inst, Dept Cardiol,Childrens Hosp,Dept Cell Biol, Boston, MA 02115 USA
[2] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
关键词
zebrafish; genetics; regeneration; fin; blastema; sly1; emmental;
D O I
10.1016/S0012-1606(03)00129-5
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Here, we used classical genetics in zebrafish to identify temperature-sensitive mutants in caudal fin regeneration. Gross morphological, histological, and molecular analyses revealed that one of these strains, emmental (emm), failed to form a functional regeneration blastema. Inhibition of emm function by heat treatment during regenerative outgrowth rapidly blocked regeneration. This block was associated with reduced proliferation in the proximal blastema and expansion of the nonproliferative distal blastemal zone. Positional cloning revealed that the emm phenotype is caused by a mutation in the orthologue of yeast sly1, a gene product involved in protein trafficking. sly1 is upregulated in the newly formed blastema as well as during regenerative outgrowth. Thus, sly1 is essential for blastemal organization and proliferation during two stages of fin regeneration. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:291 / 306
页数:16
相关论文
共 50 条
[41]   PRODUCTION OF CLONES OF HOMOZYGOUS DIPLOID ZEBRA FISH (BRACHYDANIO-RERIO) [J].
STREISINGER, G ;
WALKER, C ;
DOWER, N ;
KNAUBER, D ;
SINGER, F .
NATURE, 1981, 291 (5813) :293-296
[42]   ORGANIZATION OF HINDBRAIN SEGMENTS IN THE ZEBRAFISH EMBRYO [J].
TREVARROW, B ;
MARKS, DL ;
KIMMEL, CB .
NEURON, 1990, 4 (05) :669-679
[43]  
Tsonis PA, 1996, LIMB REGENERATION, Vxii
[44]   EXPRESSION OF ACHAETE-SCUTE HOMOLOG-3 IN XENOPUS-EMBRYOS CONVERTS ECTODERMAL CELLS TO A NEURAL FATE [J].
TURNER, DL ;
WEINTRAUB, H .
GENES & DEVELOPMENT, 1994, 8 (12) :1434-1447
[45]  
van Eeden FJM, 1999, METHOD CELL BIOL, V60, P21
[46]   Phosphorylation of histone H3 is required for proper chromosome condensation and segregation [J].
Wei, Y ;
Yu, LL ;
Bowen, J ;
Gorovsky, MA ;
Allis, CD .
CELL, 1999, 97 (01) :99-109
[47]  
Westerfield M., 2000, GUIDE LAB USE ZEBRAF
[48]   Sly1 binds to Golgi and ER syntaxins via a conserved N-terminal peptide motif [J].
Yamaguchi, T ;
Dulubova, I ;
Min, SW ;
Chen, XH ;
Rizo, J ;
Südhof, TC .
DEVELOPMENTAL CELL, 2002, 2 (03) :295-305
[49]   Activation of caspase-12, an endoplastic reticulum (ER) resident caspase, through tumor necrosis factor receptor-associated factor 2-dependent mechanism in response to the ER stress [J].
Yoneda, T ;
Imaizumi, K ;
Oono, K ;
Yui, D ;
Gomi, F ;
Katayama, T ;
Tohyama, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (17) :13935-13940
[50]   CHOP is implicated in programmed cell death in response to impaired function of the endoplasmic reticulum [J].
Zinszner, H ;
Kuroda, M ;
Wang, XZ ;
Batchvarova, N ;
Lightfoot, RT ;
Remotti, H ;
Stevens, JL ;
Ron, D .
GENES & DEVELOPMENT, 1998, 12 (07) :982-995