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Genomic organization of rat rDNA
Nucleic Acids Research
|September 24, 1983
Summary
Researchers mapped rat ribosomal DNA (rDNA) and found identical sequences in Sprague-Dawley and BD-9 rats. A significant polymorphism was identified in the non-transcribed spacer region of the 45S pre-ribosomal RNA gene.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Ribosomal DNA (rDNA) encodes ribosomal RNA (rRNA), essential for protein synthesis.
- Understanding rDNA structure and variations is crucial for studying gene regulation and evolution.
- Previous studies have characterized rDNA in various species, but detailed mapping in specific rat strains was needed.
Purpose of the Study:
- To generate a detailed restriction map of a 10.9 KB region of rat rDNA.
- To identify and characterize polymorphisms in the rDNA of Sprague-Dawley and BD-9 rats.
- To investigate repetitive DNA sequences upstream of the rRNA gene initiation site.
Main Methods:
- Restriction mapping of cloned rat rDNA and total rat DNA.
- Comparison of restriction patterns between different rat strains.
- Analysis of DNA sequences, including tandem repeats and repetitive elements.
Main Results:
- Identical rDNA restriction patterns were observed between Sprague-Dawley and BD-9 rats, and with cloned rDNA.
- A major polymorphism was identified: a 0.9 KB insertion in the non-transcribed spacer region upstream of the 45S pre-rRNA initiation site.
- This insertion region contains tandem repeats (approx. 130 bp) with poly-T tracts, similar to mouse rDNA elements.
- Highly repetitive DNA sequences were located at 2.8 KB and 4.3 KB upstream, with the 2.8 KB sequence annealing to a rat growth hormone gene-derived Alu-equivalent.
Conclusions:
- Rat rDNA sequences are highly conserved between Sprague-Dawley and BD-9 strains.
- A significant, strain-specific polymorphism exists in the non-transcribed spacer of rDNA.
- The identified repetitive elements may play roles in rDNA regulation or evolution.