Intracisternal A-particle genes in Mus musculus: a conserved family of retrovirus-like elements

1981 ◽  
Vol 1 (3) ◽  
pp. 216-227
Author(s):  
E L Kuff ◽  
L A Smith ◽  
K K Lueders

The structural organization of intracisternal A-particle genes has been studied, using isolates from a mouse gene library in lambda phage Charon 4A. The predominant gene form among the isolates was 7.3 kilobases (kb) in length. R-loops between the 7-kb (35S) A-particle genomic ribonucleic acid and several of these genes were colinear, with no visible evidence of intervening deoxyribonucleic acid sequences. One recombinant was found with an A-particle gene that contained a 1.7-kb deletion. Using the deletion as a reference, the deoxyribonucleic acid and ribonucleic acid homology regions were localized with respect to one another and to the restriction map: the 5' terminus of the ribonucleic acid was several hundred base pairs within the 5' end of the deoxyribonucleic acid homology region. Restriction endonuclease fragments encompassing the 5' and 3' regions of one 7.3-kb gene were separately subcloned into pBR322. Heteroduplexes between the two subclones revealed an approximately 300-base pair segment of terminally redundant sequences. The cloned 3' fragment hybridized with restriction fragments from the 5' end of several other A-particle genes, demonstrating the presence of common (though not necessarily identical) terminally repeated sequences. A-particle genes varied in the occurrence of specific restriction sites at characteristic internal loci. However, heteroduplexes between several variant 7.3-kb genes showed continuous homology regions even when spread under stringent hybridization conditions. The relative abundance of restriction site variants was highly conserved in 12 laboratory strains of Mus musculus, in embryonic and adult tissues of a single inbred strain, and in the SC-1 cell line of feral mouse origin, but appeared to differ in a feral Japanese substrain, Mus musculus molossinus. Some evidence suggests that subsets of A-particle genes may have similar flanking sequences. The results are discussed in terms of the evolution of this multigene family.

1981 ◽  
Vol 1 (3) ◽  
pp. 216-227 ◽  
Author(s):  
E L Kuff ◽  
L A Smith ◽  
K K Lueders

The structural organization of intracisternal A-particle genes has been studied, using isolates from a mouse gene library in lambda phage Charon 4A. The predominant gene form among the isolates was 7.3 kilobases (kb) in length. R-loops between the 7-kb (35S) A-particle genomic ribonucleic acid and several of these genes were colinear, with no visible evidence of intervening deoxyribonucleic acid sequences. One recombinant was found with an A-particle gene that contained a 1.7-kb deletion. Using the deletion as a reference, the deoxyribonucleic acid and ribonucleic acid homology regions were localized with respect to one another and to the restriction map: the 5' terminus of the ribonucleic acid was several hundred base pairs within the 5' end of the deoxyribonucleic acid homology region. Restriction endonuclease fragments encompassing the 5' and 3' regions of one 7.3-kb gene were separately subcloned into pBR322. Heteroduplexes between the two subclones revealed an approximately 300-base pair segment of terminally redundant sequences. The cloned 3' fragment hybridized with restriction fragments from the 5' end of several other A-particle genes, demonstrating the presence of common (though not necessarily identical) terminally repeated sequences. A-particle genes varied in the occurrence of specific restriction sites at characteristic internal loci. However, heteroduplexes between several variant 7.3-kb genes showed continuous homology regions even when spread under stringent hybridization conditions. The relative abundance of restriction site variants was highly conserved in 12 laboratory strains of Mus musculus, in embryonic and adult tissues of a single inbred strain, and in the SC-1 cell line of feral mouse origin, but appeared to differ in a feral Japanese substrain, Mus musculus molossinus. Some evidence suggests that subsets of A-particle genes may have similar flanking sequences. The results are discussed in terms of the evolution of this multigene family.


Genetics ◽  
1977 ◽  
Vol 86 (1) ◽  
pp. 73-84
Author(s):  
Dennis M Livingston

ABSTRACT A variety of Saccharomyces strains were examined for the presence of 2µ DNA and, if present, for the pattern of fragments produced by its digestion with site-specific (restriction) endonucleases. Two strains were found that did not contain detectable levels of 2µ DNA, and two strains contained 2µ DNA molecules having only one EcoRI restriction endonuclease recognition site rather than the usual two.—A haploid containing 2µ DNA with one EcoRI restriction site was mated with a haploid containing 2µ DNA with two EcoRI restriction sites and the resulting diploid maintained both types during vegetative growth. Sporulation of the diploid produced four spores, and the clones from these spores contained both types.—A haploid lacking 2µ DNA was mated with a haploid containing 2µ DNA and the resulting diploid contained 2µ DNA. The four clones derived from the haploid spores after sporulation of this diploid all contained 2µ DNA. A rho  - strain without 2µ DNA was mated to a rho  + strain with 2µ DNA, and heteroplasmons were selected that had received the nucleus from the strain without 2µ DNA and the mitochondria from the strain with 2µ DNA. Twelve of twenty-four such clones contained 2µ DNA.—I conclude that: (1) the different types of 2µ DNA identified in these strains do not restrict one another, (2) the different types are inherited extrachromosomally, (3) lack of 2µ DNA in two strains is not due to the absence of genes needed for maintenance and (4) the approximately 100 copies of 2µ DNA contained within a single cell are probably clustered within one or a few cytoplasmic organelles.


1966 ◽  
Vol 241 (12) ◽  
pp. 2933-2943 ◽  
Author(s):  
Abraham Novogrodsky ◽  
Moshe Tal ◽  
Abraham Traub ◽  
Jerard Hurwitz

Sign in / Sign up

Export Citation Format

Share Document