ABSTRACT
Short interspersed elements (SINEs) are one of the two most prolific mobile genomic elements in most of the higher eukaryotes. Although their biology is still not thoroughly understood, unusual life cycle of these simple elements amplified as genomic parasites makes their evolution unique in many ways. In contrast to most genetic elements including other transposons, SINEs emerged de novo many times in evolution from available molecules (for example, tRNA). The involvement of reverse transcription in their amplification cycle, huge number of genomic copies and modular structure allow variation mechanisms in SINEs uncommon or rare in other genetic elements (module exchange between SINE families, dimerization, and so on.). Overall, SINE evolution includes their emergence, progressive optimization and counteraction to the cell's defense against mobile genetic elements.
Subject(s)
DNA Transposable Elements , Eukaryota/genetics , Evolution, Molecular , Genome , Short Interspersed Nucleotide Elements , Animals , HumansABSTRACT
Here we describe a new short retroposon family of rodents. Like the primate Alu element consisting of two similar monomers, it is dimeric, but the left and right monomers are different and descend from B1 and ID short retroposons, respectively. Such elements (B1-dID) were found in the genomes of Gliridae, Sciuridae, Castoridae, Caviidae, and Hystricidae. Nucleotide sequences of this retroposon can be assigned to several structural variants. Phylogenetic analysis of B1-dID and related sequences suggests a possible scenario of B1-dID evolution in the context of rodent evolution.
Subject(s)
Phylogeny , Retroelements/genetics , Rodentia/genetics , Animals , Base Sequence , Dimerization , Molecular Sequence Data , Polymerase Chain Reaction , Sequence AlignmentABSTRACT
Band shift assays were used to study proteins from the fission yeast that bind double-stranded telomeric repeat sequences. We also examine general DNA binding properties of the telobox domain, which characterizes telomere-binding proteins from a range of species. We demonstrate that Taz1p has a high affinity for the fission yeast telomeric repeat, consistent with genetic results implicating this protein in telomere maintenance. A second Schizosaccharomyces pombe telobox protein, Teb1p, is shown to bind with high affinity to the vertebrate repeat and with low affinity to the fission yeast telomeric DNA. When tested on G-rich single-stranded telomeric DNA, all these proteins bind with very low affinity, much like the human telomere-binding protein TRF1. Recombinant proteins containing just the telobox domains reproduce the specificity of binding demonstrated for the corresponding full-length proteins, indicating that the telobox domain is indeed responsible for specific DNA recognition. The presence of possible Teb1p-binding sites upstream of many genes suggests a role for this protein as a general transcription factor. Finally, band shift experiments with whole cell extracts from wild-type and taz1 (-)strains suggest that in addition to Taz1p, S.pombe has another major telomere-binding activity.
Subject(s)
DNA, Fungal/chemistry , DNA, Fungal/metabolism , DNA-Binding Proteins/metabolism , Schizosaccharomyces pombe Proteins , Schizosaccharomyces/genetics , Schizosaccharomyces/metabolism , Telomere-Binding Proteins , Telomere/genetics , Base Sequence , Binding Sites , DNA Primers , DNA Probes , DNA-Binding Proteins/genetics , Fungal Proteins/metabolism , Genes, Fungal , Humans , Molecular Sequence Data , Polymerase Chain Reaction , Recombinant Proteins/metabolism , Repetitive Sequences, Nucleic Acid , Telomeric Repeat Binding Protein 1 , Transcription FactorsABSTRACT
Recently we described a new endogenous proretrovirus of dwarf hamster Phodopus sungorus (MRS-Ps). Its sequence possesses evident homology with the endonuclease domain of the mouse mammary tumor virus pol gene. Here we present nucleotide sequence data on three clones of retroviral long terminal repeats. As many as 15% of substituted, deleted, and inserted base pairs were found while comparing these sequences. Hence, MRS-Ps seems to be rather an old genetic element which originated about 30 million years ago. One LTR is 877 bp long and contains numerous elements that control its transcriptional activity: TATA-box, glucocorticoid responsive element, NF1-binding site, etc. Nevertheless, this LTR does not govern efficient transcription of adjacent genes in a transient expression assay. In addition, we failed to find MRS-specific mRNA in adult, embryonic, and mammary tumor cells.
Subject(s)
Cricetinae/microbiology , Genetic Variation , Proviruses/genetics , Repetitive Sequences, Nucleic Acid , Retroviridae/genetics , Transcription, Genetic , Animals , Base Sequence , Molecular Sequence Data , Plasmids , Proviruses/isolation & purification , Restriction Mapping , Retroviridae/isolation & purification , Sequence Homology, Nucleic AcidABSTRACT
Sequences (MRS) distantly related to mouse mammary tumor virus (MMTV) were found in genomes of a wide range of mammalian species using blot hybridization. The number of MRS copies and the degree of their homology with the hybridization probe varied and did not correlate with the taxonomic position of the species. Nevertheless, within a genus the set of MRS was species specific and reflected the taxonomic relation between the species. MRS were also found in avian genomes and the degree of their homology did not correlate with the taxonomic position of the species either. The origin and distribution of MRS is discussed on the basis of the authors' and published data.
