Minisatellite instability at the Adh locus reveals somatic polymorphism in amphioxus

Nucleic Acids Research

Volumn 30, Issue 13, 2002, Pages 2871-2876

  Cañestro, Cristian ^a   Gonzàlez Duarte, Roser ^a   Albalat, Ricard ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DEHYDROGENASE; DNA MINISATELLITE; MESSENGER RNA; REPETITIVE DNA; RNA;

ALLELE; ARTICLE; CHORDATA; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; EXON; GENE DUPLICATION; GENE LOCUS; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GERM LINE; INTRON; MICROSATELLITE INSTABILITY; MOLECULAR EVOLUTION; MOSAICISM; NONHUMAN; PHYLOGENY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA SPLICING; SEQUENCE ANALYSIS; SPECIES DIFFERENCE; VERTEBRATE;

ANIMALIA; BRANCHIOSTOMA; BRANCHIOSTOMA FLORIDAE; BRANCHIOSTOMA LANCEOLATUM; CEPHALOCHORDATA; CHORDATA; VERTEBRATA;

EID: 0036640527     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/gkf386     Document Type: Article

References (29)

1. Archetypal organization of the amphioxus Hox gene cluster
2. Gene duplications and the origins of vertebrate development
3. Conservation of Brachyury (T) genes in amphioxus and vertebrates: Developmental and evolutionary implications
4. Sequence and embryonic expression of the amphioxus engrailed gene (AmphiEn): The metameric pattern of transcription resembles that of its segment-polarity homolog in Drosophila
5. Characterisation of amphioxus HNF-3 genes: Conserved expression in the notochord and floor plate
6. Methylation of genomes and genes at the invertebrate-vertebrate boundary
7. The single calmodulin gene of the cephalochordate Branchiostoma
8. Differential gene expression and intracellular mRNA localization of amphioxus actin isoforms throughout development: Implications for conserved mechanisms of chordate development
9. Gene and domain duplication in the chordate Otx gene family: Insights from amphioxus Otx
10. Genomic organization and evolution of actin genes in the amphioxus Branchiostoma belcheri and Branchiostoma floridae
11. The evolution of the hedgehog gene family in chordates: Insights from amphioxus hedgehog
12. Characterization of an amphioxus paired box gene, AmphiPax2/5/8: Developmental expression patterns in optic support cells, nephridium, thyroid-like structures and pharyngeal gill slits, but not in the region
13. Amphioxus alcohol dehydrogenase is a class 3 form of single type and of structural conservation but with unique developmental expression
14. Left-right asymmetric expression of BbPtx, a Ptx-related gene, in a lancelet species and the developmental left-sidedness in deuterostomes
15. Characterization of a microsomal retinol dehydrogenase gene from amphioxus: Retinoid metabolism before vertebrates
16. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA
17. Complex gene conversion events in germline mutation at human minisatellites
18. Somatic mutation processes at a human minisatellite
19. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
20. Genomic organization and expression of the planarian homeobox genes Dth-1 and Dth-2
21. Ascidian and Amphioxus Adh genes correlate functional and molecular features of the ADH family expansion during vertebrate evolution
22. Simple sequences and the expanding genome
23. The evolutionary dynamics of repetitive DNA in eukaryotes
24. Eukaryotic DNA methylation as an evolutionary device
25. Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice
26. Characterization of the amphioxus presenilin gene in a high gene-density genomic region illustrates duplication during the vertebrate lineage
27. Complex patterns of intragenic polymorphism at the PDGFA locus
28. Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: A single nucleotide substitution in the second repeat prevents multiple alternate splicing
29. Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)