Mannose 6-phosphate receptors in an ancient vertebrate, zebrafish

被引:20
作者
Nolan, CM [1 ]
McCarthy, K
Eivers, E
Jirtle, RL
Byrnes, L
机构
[1] Univ Coll Dublin, Sch Biol & Environm Sci, Dublin 4, Ireland
[2] Natl Univ Ireland Univ Coll Galway, Dept Biochem, Galway, Ireland
[3] Duke Univ, Sch Med, Dept Radiat Oncol, Durham, NC USA
关键词
D O I
10.1007/s00427-005-0046-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endosome/lysosome system plays key roles in embryonic development, but difficulties posed by inaccessible mammalian embryos have hampered detailed studies. The accessible, transparent embryos of Danio rerio, together with the genetic and experimental approaches possible with this organism, provide many advantages over rodents. In mammals, mannose 6-phosphate receptors (MPRs) target acid hydrolases to endosomes and lysosomes, but nothing is known of acid hydrolase targeting in zebrafish. Here, we describe the sequence of the zebrafish cation-dependent MPR (CD-MPR) and cation-independent MPR (CI-MPR), and compare them with their mammalian orthologs. We show that all residues critical for mannose 6-phosphate (M6P) recognition are present in the extracellular domains of the zebrafish receptors, and that trafficking signals in the cytoplasmic tails are also conserved. This suggests that the teleost receptors possess M6P binding sites with properties similar to those of mammalian MPRs, and that targeting of lysosomal enzymes by MPRs represents an ancient pathway in vertebrate cell biology. We also determined the expression patterns of the CD-MPR and CI-MPR during embryonic development in zebrafish. Both genes are expressed from the one-cell stage through to the hatching period. In early embryos, expression is ubiquitous, but in later stages, expression of both receptors is restricted to the anterior region of the embryo, covering the forebrain, midbrain and hindbrain. The expression patterns suggest time- and tissue-specific functions for the receptors, with particular evidence for roles in neural development. Our study establishes zebrafish as a novel, genetically tractable model for in vivo studies of MPR function and lysosome biogenesis.
引用
收藏
页码:144 / 151
页数:8
相关论文
共 20 条
[1]   Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor [J].
Arighi, CN ;
Hartnell, LM ;
Aguilar, RC ;
Haft, CR ;
Bonifacino, JS .
JOURNAL OF CELL BIOLOGY, 2004, 165 (01) :123-133
[2]   Structure of a functional IGF2R fragment determined from the anomalous scattering of sulfur [J].
Brown, J ;
Esnouf, RM ;
Jones, MA ;
Linnell, J ;
Harlos, K ;
Hassan, AB ;
Jones, EY .
EMBO JOURNAL, 2002, 21 (05) :1054-1062
[3]   P-type lectins [J].
Dahms, NM ;
Hancock, MK .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2002, 1572 (2-3) :317-340
[4]   The novel Drosophila lysosomal enzyme receptor protein mediates lysosomal sorting in mammalian cells and binds mammalian and Drosophila GGA adaptors [J].
Dennes, A ;
Cromme, C ;
Suresh, K ;
Kumar, NS ;
Eble, JA ;
Hahnenkamp, A ;
Pohlmann, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (13) :12849-12857
[5]   Insulin-like growth factor (IGF) signalling is required for early dorso-anterior development of the zebrafish embryo [J].
Eivers, E ;
McCarthy, K ;
Glynn, C ;
Nolan, CM ;
Byrnes, L .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2004, 48 (10) :1131-1140
[6]   Mannose 6-phosphate receptors: New twists in the tale [J].
Ghosh, P ;
Dahms, NM ;
Kornfeld, S .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (03) :202-212
[7]  
JADOT M, 1992, J BIOL CHEM, V267, P11069
[8]   M6P/IGF2R imprinting evolution in mammals [J].
Killian, JK ;
Byrd, JC ;
Jirtle, JV ;
Munday, BL ;
Stoskopf, MK ;
MacDonald, RG .
MOLECULAR CELL, 2000, 5 (04) :707-716
[9]   STRUCTURE AND FUNCTION OF THE MANNOSE 6-PHOSPHATE INSULIN-LIKE GROWTH FACTOR-II RECEPTORS [J].
KORNFELD, S .
ANNUAL REVIEW OF BIOCHEMISTRY, 1992, 61 :307-330
[10]   A FUNCTIONALLY CONSERVED HOMOLOGY OF THE DROSOPHILA SEGMENT POLARITY GENE-HH IS EXPRESSED IN TISSUES WITH POLARIZING ACTIVITY IN ZEBRAFISH EMBRYOS [J].
KRAUSS, S ;
CONCORDET, JP ;
INGHAM, PW .
CELL, 1993, 75 (07) :1431-1444