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Cloned endogenous retroviral sequences from human DNA
Summary
Researchers identified a human retroviral sequence homologous to baboon endogenous virus and Moloney murine leukemia virus. This ancient sequence, found in both human and chimpanzee genomes, predates their evolutionary divergence.
Area of Science:
- Molecular Biology
- Genomics
- Evolutionary Biology
Background:
- Endogenous retroviruses (ERVs) are remnants of ancient viral infections integrated into host genomes.
- Comparative genomics can reveal evolutionary relationships and ancient genetic elements.
- Human and primate genomes harbor diverse retroviral sequences of varying evolutionary ages.
Purpose of the Study:
- To identify and characterize novel human endogenous retroviral sequences.
- To investigate the evolutionary origins and conservation of specific retroviral elements in primates.
- To determine the genomic copy number and chromosomal location of a newly identified human retroviral sequence.
Main Methods:
- Screening of a human DNA library using a chimpanzee retroviral probe.
- DNA sequencing and sequence homology analysis of cloned human DNA fragments.
- Hybridization of cloned DNA to human genomic DNA digests (Southern blotting).
Main Results:
- A 20-kilobase human DNA sequence with homology to baboon endogenous virus polymerase gene was identified.
- The human sequence contains homologous regions to gag p30, gag p15, and polymerase genes of Moloney murine leukemia virus, with conserved spacing.
- The human genome contains two closely related copies and approximately ten less related copies of this retroviral sequence.
- Identical 3' flanking sequences in human and chimpanzee clones suggest the retroviral element predates human-chimpanzee divergence.
Conclusions:
- A novel human endogenous retroviral sequence, sharing homology with known retroviruses, has been identified.
- The conserved structure and flanking sequences indicate this retroviral element is ancient and shared between humans and chimpanzees.
- This finding provides insights into the integration and evolutionary history of retroviruses in primate genomes.