Classical and molecular cytogenetics of the pufferfish tetraodon nigroviridis

被引:28
作者
Grützner, F
Lütjens, G
Rovira, C
Barnes, DW
Ropers, HH
Haaf, T
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Karolinska Inst, Novum, Dept Biosci, S-14157 Huddinge, Sweden
[3] ATCC, Manassas, VA 20110 USA
关键词
FISH; Fugu rubripes; heterochromatin; Huntingtin; NOR; pufferfish; replication banding; Tetraodon nigroviridis;
D O I
10.1023/A:1009292220760
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Because of its highly compact genome, the pufferfish has become an important animal model in genome research. Although the small chromosome size renders chromosome analysis difficult, we have established both classical and molecular cytogenetics in the freshwater pufferfish Tetraodon nigroviridis (TNI). The karyotype of T. nigroviridis consists of 2n = 42 biarmed chromosomes, in contrast to the known 2n = 44 chromosomes of the Japanese pufferfish Fugu rubripes (FRU). RBA banding can identify homologous chromosomes in both species. TNI 1 corresponds to two smaller FRU chromosomes, explaining the difference in chromosome number. TNI 2 is homologous to FRU 1. Fluorescence in-situ hybridization (FISH) allows one to map single-copy sequences, i.e. the Huntingtin gene, on chromosomes of the species of origin and also on chromosomes of the heterologous pufferfish species. Hybridization of total genomic DNA shows large blocks of (species-specific) repetitive sequences in the pericentromeric region of all TNI and FRU chromosomes. Hybridization with cloned human rDNA and classical silver staining reveal two large and actively transcribed rRNA gene clusters. Similar to the situation in mammals, the highly compact pufferfish genome is endowed with considerable amounts of localized repeat DNAs.
引用
收藏
页码:655 / 662
页数:8
相关论文
共 37 条
[1]  
Arai R., 1983, Bulletin of the National Science Museum Series A (Zoology), V9, P175
[2]   The comparative genomic structure and sequence of the surfeit gene homologs in the puffer fish Fugu rubripes and their association with CpG-rich islands [J].
Armes, N ;
Gilley, J ;
Fried, M .
GENOME RESEARCH, 1997, 7 (12) :1138-1152
[3]  
BARAT A, 1984, CURR SCI INDIA, V53, P1108
[4]   COMPARATIVE SEQUENCE-ANALYSIS OF THE HUMAN AND PUFFERFISH HUNTINGTONS-DISEASE GENES [J].
BAXENDALE, S ;
ABDULLA, S ;
ELGAR, G ;
BUCK, D ;
BERKS, M ;
MICKLEM, G ;
DURBIN, R ;
BATES, G ;
BRENNER, S ;
BECK, S ;
LEHRACH, H .
NATURE GENETICS, 1995, 10 (01) :67-76
[5]   THE ISOCHORE ORGANIZATION OF THE HUMAN GENOME [J].
BERNARDI, G .
ANNUAL REVIEW OF GENETICS, 1989, 23 :637-661
[6]   IMPROVED TECHNIQUE FOR SELECTIVE SILVER STAINING OF NUCLEOLAR ORGANIZER REGIONS IN HUMAN-CHROMOSOMES [J].
BLOOM, SE ;
GOODPASTURE, C .
HUMAN GENETICS, 1976, 34 (02) :199-206
[7]  
Bradford CS, 1997, MOL MAR BIOL BIOTECH, V6, P279
[8]   CHARACTERIZATION OF THE PUFFERFISH (FUGU) GENOME AS A COMPACT MODEL VERTEBRATE GENOME [J].
BRENNER, S ;
ELGAR, G ;
SANDFORD, R ;
MACRAE, A ;
VENKATESH, B ;
APARICIO, S .
NATURE, 1993, 366 (6452) :265-268
[9]  
Brunner B, 1999, GENOME RES, V9, P437
[10]   MITOGENIC ACTIVITY FROM TROUT EMBRYOS [J].
COLLODI, P ;
BARNES, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3498-3502