Literature DB >> 21364693

The linked units of 5S rDNA and U1 snDNA of razor shells (Mollusca: Bivalvia: Pharidae).

J Vierna1, K T Jensen, A Martínez-Lage, A M González-Tizón.   

Abstract

The linkage between 5S ribosomal DNA and other multigene families has been detected in many eukaryote lineages, but whether it provides any selective advantage remains unclear. In this work, we report the occurrence of linked units of 5S ribosomal DNA (5S rDNA) and U1 small nuclear DNA (U1 snDNA) in 10 razor shell species (Mollusca: Bivalvia: Pharidae) from four different genera. We obtained several clones containing partial or complete repeats of both multigene families in which both types of genes displayed the same orientation. We provide a comprehensive collection of razor shell 5S rDNA clones, both with linked and nonlinked organisation, and the first bivalve U1 snDNA sequences. We predicted the secondary structures and characterised the upstream and downstream conserved elements, including a region at -25 nucleotides from both 5S rDNA and U1 snDNA transcription start sites. The analysis of 5S rDNA showed that some nontranscribed spacers (NTSs) are more closely related to NTSs from other species (and genera) than to NTSs from the species they were retrieved from, suggesting birth-and-death evolution and ancestral polymorphism. Nucleotide conservation within the functional regions suggests the involvement of purifying selection, unequal crossing-overs and gene conversions. Taking into account this and other studies, we discuss the possible mechanisms by which both multigene families could have become linked in the Pharidae lineage. The reason why 5S rDNA is often found linked to other multigene families seems to be the result of stochastic processes within genomes in which its high copy number is determinant.

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Year:  2011        PMID: 21364693      PMCID: PMC3178405          DOI: 10.1038/hdy.2010.174

Source DB:  PubMed          Journal:  Heredity (Edinb)        ISSN: 0018-067X            Impact factor:   3.821


  66 in total

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4.  Transcription termination by nuclear RNA polymerases.

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5.  The 5S gene internal control region is composed of three distinct sequence elements, organized as two functional domains with variable spacing.

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6.  The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.

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8.  Nucleotide sequences in Xenopus 5S DNA required for transcription termination.

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  9 in total

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Journal:  J Mol Evol       Date:  2012-07-11       Impact factor: 2.395

2.  Systematic analysis and evolution of 5S ribosomal DNA in metazoans.

Authors:  J Vierna; S Wehner; C Höner zu Siederdissen; A Martínez-Lage; M Marz
Journal:  Heredity (Edinb)       Date:  2013-07-10       Impact factor: 3.821

3.  The 5S rDNA in two Abracris grasshoppers (Ommatolampidinae: Acrididae): molecular and chromosomal organization.

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Journal:  Mol Genet Genomics       Date:  2016-04-22       Impact factor: 3.291

4.  Isolation and characterization of 5S rDNA sequences in catfishes genome (Heptapteridae and Pseudopimelodidae): perspectives for rDNA studies in fish by C0t method.

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Journal:  Cytotechnology       Date:  2016-06-25       Impact factor: 2.058

5.  U1 snDNA clusters in grasshoppers: chromosomal dynamics and genomic organization.

Authors:  A Anjos; F J Ruiz-Ruano; J P M Camacho; V Loreto; J Cabrero; M J de Souza; D C Cabral-de-Mello
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6.  Molecular organization and phylogenetic analysis of 5S rDNA in crustaceans of the genus Pollicipes reveal birth-and-death evolution and strong purifying selection.

Authors:  Alejandra Perina; David Seoane; Ana M González-Tizón; Fernanda Rodríguez-Fariña; Andrés Martínez-Lage
Journal:  BMC Evol Biol       Date:  2011-10-17       Impact factor: 3.260

7.  The cnidarian Hydractinia echinata employs canonical and highly adapted histones to pack its DNA.

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8.  Evolutionary dynamics of rRNA gene clusters in cichlid fish.

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9.  Contrasting the Chromosomal Organization of Repetitive DNAs in Two Gryllidae Crickets with Highly Divergent Karyotypes.

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  9 in total

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