Comparison of the sequence organization of related retrovirus-like multigene families in three evolutionary distant rodent genomes

Sequences related to mouse intracisternal A-particle (IAP) genes have been isolated from rat and Syrian hamster gene libraries as recombinants in λ phage. The sequences are moderately reiterated in both these genomes but their sequence organization in the hamster genome is different from that in the...

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Bibliographic Details
Published inNucleic acids research Vol. 11; no. 13; pp. 4391 - 4408
Main Authors Lueders, Kira K., Kuff, Edward L.
Format Journal Article
LanguageEnglish
Published Oxford University Press 11.07.1983
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Summary:Sequences related to mouse intracisternal A-particle (IAP) genes have been isolated from rat and Syrian hamster gene libraries as recombinants in λ phage. The sequences are moderately reiterated in both these genomes but their sequence organization in the hamster genome is different from that in the rat genome. Restriction analysis and electron microscopy indicate that the Syrian hamster IAP sequences represent a family of relatively homogeneous well-conserved units; in this, they resemble the mouse IAP genes. The rat sequences, in contrast, are heterogeneous. Both the hamster and rat IAP sequences contain regions homologous to mouse IAP genes interspersed with regions of apparent non-homology. The interspersed regions range in size from 0.5–1.0 kilobases (Kb). The regions of homology among the mouse, rat and Syrian hamster IAP sequences have been mapped to a 5–6 Kb internal region on the mouse IAP genes. Mouse IAP long terminal repeat (LTR) sequences were not detected in the rat and Syrian hamster genomes. We used the thermal stability of hybrids between cloned and genomic LAP sequences to measure family homogeneity. Mouse and Syrian hamster IAP sequences are homogeneous by this criterion, but the rat IAP sequences are heterogeneous with a Tm 6°C below the self-hybrid. The contrasting organization of IAP-related elements in the genomes of these rodents indicates that amplification or homogenization of this sequence family has occurred independently and at different periods of time during their evolution.
Bibliography:ArticleID:11.13.4391
ark:/67375/HXZ-L55ZST4H-K
Author to whom requests for reprints should be addressed
istex:131327B3F4B5654D70F645BBB0A762644055EE18
ISSN:0305-1048
1362-4962
DOI:10.1093/nar/11.13.4391