Literature DB >> 24317895

Repeat sequence interspersion in coding DNA of peas does not reflect that in total pea DNA.

M G Murray1, W F Thompson.   

Abstract

The pattern of sequence organization in the regions of the pea genome near sequences coding for mRNA differs significantly from that in total DNA. Interspersion of repeated and single copy sequences is so extensive that 85% of 1300 nucleotide-long fragments contain highly repetitive sequences (about 5000 copies per haploid genome). However, data presented here demonstrate that sequences which code for mRNA are enriched in the small fraction of fragments which do not contain these highly repetitive sequences. Thus, in contrast to the great majority of other sequences in the genome, most mRNA coding sequences are not located within 1300 nucleotides of highly repetitive elements. Moreover, our data indicate that those repeats (if any) which are closely associated with mRNA coding sequences belong to low copy number families characterized by an unusually low degree of sequence divergence.

Entities:  

Year:  1982        PMID: 24317895     DOI: 10.1007/BF00024977

Source DB:  PubMed          Journal:  Plant Mol Biol        ISSN: 0167-4412            Impact factor:   4.076


  21 in total

Review 1.  Hybridization and renaturation kinetics of nucleic acids.

Authors:  J G Wetmur
Journal:  Annu Rev Biophys Bioeng       Date:  1976

2.  Structural genes adjacent to interspersed repetitive DNA sequences.

Authors:  E H Davidson; B R Hough; W H Klein; R J Britten
Journal:  Cell       Date:  1975-03       Impact factor: 41.582

3.  A program for least squares analysis of reassociation and hybridization data.

Authors:  W R Pearson; E H Davidson; R J Britten
Journal:  Nucleic Acids Res       Date:  1977-06       Impact factor: 16.971

4.  Gene regulation for higher cells: a theory.

Authors:  R J Britten; E H Davidson
Journal:  Science       Date:  1969-07-25       Impact factor: 47.728

5.  Message sequences and short repetitive sequences are interspersed in sea urchin egg poly(A)+ RNAs.

Authors:  F D Costantini; R J Britten; E H Davidson
Journal:  Nature       Date:  1980-09-11       Impact factor: 49.962

6.  Evolutionary sequence divergence within repeated DNA families of higher plant genomes. II. Analysis of thermal denaturation.

Authors:  R S Preisler; W F Thompson
Journal:  J Mol Evol       Date:  1981       Impact factor: 2.395

7.  The single-copy DNA sequence polymorphism of the sea urchin Strongylocentrotus purpuratus.

Authors:  R J Britten; A Cetta; E H Davidson
Journal:  Cell       Date:  1978-12       Impact factor: 41.582

8.  Deoxyribonucleic acid sequence organization in the mung bean genome.

Authors:  M G Murray; J D Palmer; R E Cuellar; W F Thompson
Journal:  Biochemistry       Date:  1979-11-13       Impact factor: 3.162

9.  Preferential expression of unique sequences adjacent to middle repetitive sequences in mouse cytoplasmic RNA.

Authors:  A Kuroiwa; S Natori
Journal:  Nucleic Acids Res       Date:  1979-10-10       Impact factor: 16.971

10.  Aggregate formation from short fragments of plant DNA.

Authors:  W F Thompson
Journal:  Plant Physiol       Date:  1976-04       Impact factor: 8.340

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  2 in total

1.  Insertional polymorphism and antiquity of PDR1 retrotransposon insertions in pisum species.

Authors:  Runchun Jing; Maggie R Knox; Jennifer M Lee; Alexander V Vershinin; Michael Ambrose; T H Noel Ellis; Andrew J Flavell
Journal:  Genetics       Date:  2005-08-05       Impact factor: 4.562

2.  Comparative analysis of genetic diversity in pea assessed by RFLP- and PCR-based methods.

Authors:  J Lu; M R Knox; M J Ambrose; J K Brown; T H Ellis
Journal:  Theor Appl Genet       Date:  1996-11       Impact factor: 5.699

  2 in total

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