Endogenous
retroviruses (ERVs) are LTR (Long Terminal Repeats) retroelements, present mostly
in human and other mammal’s genomes, making up, for example, 4,7 % of the human
genome. ERVs differ from the conventional LTR retroelements, because they
resemble more decayed viral retroelements rather than true transposons.
ERVs are
very similar to conventional retrotransposons, because in both cases there’s
the involvement of a RNA intermediate. The difference is that in transcription
mechanisms in retrotransposition the RNA molecule has an endogenous origin,
being transcribed from its own genome, while in retroviral replication
mechanisms, transcription occurs from an exogenous viral genome.
ERVs are
permanent constituents of the host’s genome, and are inherited from generation
to generation, like any other constituent of the host’s genome. Retroviral infections
normally attack somatic cells, but in the ERV’s case, it is thought that this
genomic integration is the result of retroviral infection of germ cells, which
resulted in its integration and transmission to subsequent generations. That’s
why the term “endogenous retroviruses” is used.
In the
human genome, ERVs possess copies of the genes gag, pol and env, but however most ERVs suffered
mutations or deletions which inactivated one or more of these genes, which
resulted in the loss of its viral replication activity. The majority of ERVs are
therefore inactive sequences that are not capable of additional proliferation as
retrotransposons.
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