Organization of the 5S ribosomal RNA genes in the genome of tomato

Genome ◽  
1991 ◽  
Vol 34 (4) ◽  
pp. 509-514 ◽  
Author(s):  
Nora L. V. Lapitan ◽  
Martin W. Ganal ◽  
Steven D. Tanksley

The 5S ribosomal RNA (rRNA) genes represent one of the most abundant gene families in eukaryotic genomes and have been a model system for the study of molecular organization and evolution of multigene families in eukaryotes. This paper reports a detailed characterization of the 5S rRNA genes of tomato (Lycopersicon esculentum) with respect to chromosome assignment, chromosomal localization, copy number, and physical size. By restriction fragment length polymorphism, the tandemly repeated 5S rRNA genes were assigned to a region of chromosome 1 of tomato. These results were confirmed by in situ hybridization onto tomato metaphase chromosomes. The single hybridization signal was localized to the short arm of chromosome 1, in a region close to the centromere. Based on reconstruction experiments, it was estimated that the 400-bp repeating unit occurs in approximately 1000 copies per haploid genome. Physical characterization of the entire locus was then performed by means of pulsed-field gel electrophoresis. Digestion of high molecular weight DNA of tomato with restriction enzymes such as PvuII, ClaI, and BglII resulted in a very prominent band with a size between approximately 450 and 600 kb. This value closely matched the estimated size of the gene cluster based on reconstruction experiments. The data therefore suggest that all the 5S rRNA genes in tomato occur in a single, continuous array, uninterrupted by unrelated sequences.Key words: 5S rRNA genes, organization, Lycopersicon esculentum, in situ hybridization, pulsed-field gel electrophoresis.

1994 ◽  
Vol 66 (4) ◽  
pp. 246-249 ◽  
Author(s):  
Y. Matsuda ◽  
K. Moriwaki ◽  
V.M. Chapman ◽  
Y. Hoi-Sen ◽  
J. Akbarzadeh ◽  
...  

Hereditas ◽  
2004 ◽  
Vol 124 (1) ◽  
pp. 95-97 ◽  
Author(s):  
Clemens H. M. Mellink ◽  
Anneke A. Bosma ◽  
Nel A. Haan ◽  
Carla Zijlstra

Genome ◽  
1995 ◽  
Vol 38 (3) ◽  
pp. 623-626 ◽  
Author(s):  
Angeles Cuadrado ◽  
Nicolas Jouv ◽  
J. S. Heslop-Harrison

In situ hybridization was used to physically map the 5S rRNA multigene family in three selected lines of hexaploid triticale and five lines of diploid rye. Using this technique, evidence for a new locus on the 3RS arm of the three triticale lines was first obtained, as well as confirmation of the presence of 5S rRNA loci on wheat and rye chromosomes of homoeologous groups 1 and 5. The new locus on the 3RS arm was confirmed in two lines of rye, Secale cereale L., although it was not present in the other rye varieties studied. We propose that the new 5S rRNA locus be referred to as 5SDna-R3.Key words: in situ hybridization, FISH, Secale, triticale, 5S rRNA genes.


Gene ◽  
1994 ◽  
Vol 142 (2) ◽  
pp. 291-295 ◽  
Author(s):  
Charlotte Hallenberg ◽  
Jens <SNM> Nederby Nielsen ◽  
Sune Frederiksen
Keyword(s):  
5S Rrna ◽  

1993 ◽  
Vol 63 (3) ◽  
pp. 144-146 ◽  
Author(s):  
B. Heckl-&Ouml;streicher ◽  
S. Ragg ◽  
M. Drechsler ◽  
H. Scherthan ◽  
B. Royer-Pokora

Genome ◽  
1997 ◽  
Vol 40 (2) ◽  
pp. 171-175 ◽  
Author(s):  
J. Schondelmaier ◽  
T. Schmidt ◽  
C. Jung ◽  
J. S. Heslop-Harrison

A digoxigenin-labelled 5S rDNA probe containing the 5S rRNA gene and the adjacent intergenic spacer was used for in situ hybridization to metaphase and interphase chromosomes of a trisomic stock from sugar beet (Beta vulgaris L.). Three chromosomes of primary trisomic line IV (T. Butterfass. Z. Bot. 52: 46–77. 1964) revealed signals close to the centromeres. Polymorphisms of 5S rDNA repeats in a segregating population were used to map genetically the 5S rRNA genes within a cluster of markers in linkage group II of sugar beet. The concentration of genetic markers around the centromere presumably reflects the suppressed recombination frequency in centromeric regions. The correlation of physical and genetic data allowed the assignment of a linkage group to sugar beet chromosome IV according to line IV of the primary trisomics.Key words: Beta vulgaris, sugar beet, 5S rRNA, in situ hybridization, RFLPs, trisomics.


2007 ◽  
Vol 53 (1) ◽  
pp. 116-128 ◽  
Author(s):  
Richard Villemur ◽  
Philippe Constant ◽  
Annie Gauthier ◽  
Martine Shareck ◽  
Réjean Beaudet

Strains of Desulfitobacterium hafniense, such as strains PCP-1, DP7, TCE1, and TCP-A, have unusual long 16S ribosomal RNA (rRNA) genes due to an insertion of approximately 100 bp in the 5' region. In this report, we analyzed the 16S rRNA genes of different Desulfitobacterium strains to determine if such an insertion is a common feature of desulfitobacteria. We amplified this region by polymerase chain reaction (PCR) from eight Desulfitobacterium strains (D. hafniense strains PCP-1, DP7, TCP-A, TCE1, and DCB-2; D. dehalogenans; D. chlororespirans; and Desulfitobacterium sp. PCE1) and resolved each PCR product by denaturing gradient gel electrophoresis (DGGE). All strains had from two to seven DGGE- migrating bands, suggesting heterogeneity in their 16S rRNA gene copies. For each strain, the 5' region of the 16S rRNA genes was amplified and a clone library was derived. Clones corresponding to most PCR–DGGE migration bands were isolated. Sequencing of representative clones revealed that the heterogeneity was generated by insertions of 100–200 bp. An insertion was found in at least one copy of the 16S rRNA gene in all examined strains. In total, we found eight different types of insertions (INS1–INS8) that varied from 123 to 193 nt in length. Two-dimensional structural analyses of transcribed sequences predicted that all insertions would form an energetically stable loop. Reverse transcriptase – PCR experiments revealed that most of the observed insertions in the Desulfitobacterium strains were excised from the mature 16S rRNA transcripts. Insertions were not commonly found in bacterial 16S rRNA genes, and having a different insertion in several 16S rRNA gene copies borne by a single bacterial species was rarely observed. The function of these insertions is not known, but their occurrence can have an important impact in deriving 16S rRNA oligonucleotidic fluorescence in situ hybridization probes, as these insertions can be excised from 16S rRNA transcripts.Key words: Desulfitobacterium, 16S ribosomal RNA genes, heterogeneity, gene insertions, fluorescence in situ hybridization.


1991 ◽  
Vol 19 (15) ◽  
pp. 4147-4151 ◽  
Author(s):  
Pernill Dissing Sørensen ◽  
Sune Frederiksen
Keyword(s):  
5S Rrna ◽  

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