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Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs).

Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Research Abstract Details 

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  • Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Abstract Text:

    maren krullMaren Krull,mirjan petrusmaMirjan Petrusma,wojciech makalowskiWojciech Makalowski, brosius Brosius, schmitz Schmitz,

    Exonization of retroposed mobile elements, a process whereby new exons are generated following changes in non-protein-coding regions of a gene, is thought to have great potential for generating proteins with novel domains. Our previous analysis of primate-specific Alu-short interspersed elements (SINEs) showed, however, that during their 60 million years of evolution, SINE exonizations occurred in some primates, only to be lost again in some of the descendent lineages. This dynamic gain and loss makes it difficult to ascertain the contribution of exonization to genomic novelty. It was speculated that Alu-SINEs are too young to reveal persistent protein exaptation. In the present study we examined older mobile elements, mammalian-wide interspersed repeats (MIRs) that underwent active retroposition prior to the placental mammalian radiation approximately 130 million years ago, to determine their contribution to protein-coding sequences. Of 107 potential cases of MIR exonizations in human, an analysis of splice sites substantiates a mechanism that benefits from 3' splice site selection in MIR sequences. We retraced in detail the evolution of five MIR elements that exonized at different times during mammalian evolution. Four of these are expressed as alternatively spliced transcripts; three in species throughout the mammalian phylogenetic tree and one solely in primates. The fifth is the first experimentally verified, constitutively expressed retroposed SINE element in mammals. This pattern of highly conserved, alternatively and constitutively spliced MIR sequences evinces the potential of exonized transposed elements to evolve beyond the transient state found in Alu-SINEs and persist as important parts of functional proteins.

    Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Publishing Authors By Initials

    m krullM Krull,m petrusmaM Petrusma,w makalowskiW Makalowski,j brosiusJ Brosius,j schmitzJ Schmitz,

    For similar nucleic acids, nucleotides, and nucleosides: nucleic acids: dna: retroelements research abstracts see: nucleic acids, nucleotides, and nucleosides: nucleic acids: dna: retroelements research

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    Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Genome research

    VOLUME: 17

    Page Numbers: 1139-45

    Journal Abbreviation: Genome Res.

    ISSN: 1088-9051

    DAY: 10

    MONTH: 07

    YEAR: 2007

    Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9518021

    Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Keywords Mesh Terms:

    KEYWORDS: Retroelements

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs). Information

    Substance Name: Retroelements

    Registry Number: 0

    Grant and Affiliation Information for Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs).

    AFFILIATION: Institute of Experimental Pathology (ZMBE), University of Münster, Münster, Germany.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Genome Res

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