Literature DB >> 8605993

Pseudogenes in ribonuclease evolution: a source of new biomacromolecular function?

N Trabesinger-Ruef1, T Jermann, T Zankel, B Durrant, G Frank, S A Benner.   

Abstract

Bovine seminal ribonuclease (RNase) diverged from pancreatic RNase after a gene duplication ca. 35 million years ago. Members of the seminal RNase gene family evidently remained as unexpressed pseudogene for much of its evolutionary history. Between 5 and 10 million years ago, however, after the divergence of kudu but before the divergence of ox, evidence suggests that the pseudogene was repaired and expressed. Intriguingly, detailed analysis of the sequences suggests that the repair may have involved gene conversion, transfer of information from the pancreatic gene to the RNase pseudogene. Further, the ratio of non-silent to silent substitutions suggests that the pancreatic RNases are divergently evolving under functional constraints, the seminal RNase pseudogenes are diverging under no functional constraints, while the genes expressed in the seminal plasma are evolving extremely rapidly in their amino acid sequences, as if to fulfil a new physiological role.

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Year:  1996        PMID: 8605993     DOI: 10.1016/0014-5793(96)00191-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  11 in total

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5.  Snake venom disintegrins: novel dimeric disintegrins and structural diversification by disulphide bond engineering.

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6.  Transcribed processed pseudogenes in the human genome: an intermediate form of expressed retrosequence lacking protein-coding ability.

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7.  The adaptive evolution database (TAED).

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Review 8.  Eosinophil-Derived Neurotoxin (EDN/RNase 2) and the Mouse Eosinophil-Associated RNases (mEars): Expanding Roles in Promoting Host Defense.

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9.  Analysis of transitions at two-fold redundant sites in mammalian genomes. Transition redundant approach-to-equilibrium (TREx) distance metrics.

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10.  Activation of the Arabidopsis thaliana immune system by combinations of common ACD6 alleles.

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Journal:  PLoS Genet       Date:  2014-07-10       Impact factor: 5.917

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