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1.
Genome ; 43(3): 538-49, 2000 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10902719

RESUMO

We estimated recombination rates between 312 loci and their centromeres in gynogenetic diploid pink salmon (Oncorhynchus gorbuscha) that we produced by initiating development with irradiated sperm and blocking the maternal second meiotic division. Amplified fragment length polymorphisms (AFLPs) were significantly more centromeric than loci identified by three other techniques (allozymes, microsatellites, and PCR using primer sequences from interspersed nuclear elements). The near absence of AFLPs in distal regions could limit their utility in constructing linkage maps. A large proportion of loci had frequency of second division segregation (y) values approaching 1.0, indicating near complete crossover interference on many chromosome arms. As predicted from models of chromosomal evolution in salmonids based upon results with allozyme loci, all duplicated microsatellite loci that shared alleles (isoloci) had y values of nearly 1.0.


Assuntos
Centrômero/genética , Salmão/genética , Animais , Mapeamento Cromossômico , Troca Genética , Marcadores Genéticos , Meiose , Repetições de Microssatélites , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Retroelementos , Telômero/genética
2.
J Hered ; 90(2): 289-96, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10070777

RESUMO

We describe the inheritance of 460 PCR-based loci in the polyploid-derived pink salmon (Oncorhynchus gorbuscha) genome using gynogenetic haploid embryos. We detected a length polymorphism in a growth hormone gene (GH-2) intron that is caused by an 81 bp insertion homologous to the 3' end of the salmonid short interspersed repetitive element (SINE) SmaI. Such insertion polymorphisms within species bring into question the use of SINEs as phylogenetic markers. We confirmed that a microsatellite locus encodes a PCR-null allele that is responsible for an apparent deficit of heterozygotes in a population sample from Prince William Sound. Another set of microsatellite primers amplified alleles of the same molecular weight from both loci of a duplicated pair. In our analysis of several PCR-based multilocus techniques, we failed to detect evidence of comigrating fragments produced by duplicated loci. Segregation analysis of PCR-based markers using gynogenetic haploid embryos ensures that the interpretation of molecular variation is not complicated by heterozygosity, diploidy, or gene duplication. We urge investigators to test the inheritance of polymorphisms in salmonids prior to using them to measure genetic variation.


Assuntos
Núcleo Celular/metabolismo , Marcadores Genéticos/genética , Salmão/genética , Animais , Sequência de Bases , DNA , Primers do DNA , Duplicação Gênica , Hormônio do Crescimento/genética , Repetições de Microssatélites , Dados de Sequência Molecular , Retroelementos
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