Related Experiment Video
Updated: May 6, 2026

13:16
Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
Published on: January 22, 2018
23.3K
A novel repetitive DNA sequence in the genus Oryza
Summary
Researchers characterized a novel repetitive DNA sequence, CC-1, in rice. This finding enhances understanding of rice genome organization and evolutionary relationships among different rice genomes.
Area of Science:
- Genomics
- Molecular Biology
- Plant Science
Background:
- Repetitive DNA sequences constitute a significant portion of the nuclear DNA in the genus Oryza (rice).
- Understanding these repetitive elements is crucial for deciphering rice genome organization and evolutionary history.
Purpose of the Study:
- To isolate and characterize a novel repetitive DNA sequence, designated CC-1, from the CC genome of rice.
- To investigate the distribution, copy number, and structural variations of the CC-1 sequence across different rice genomes.
Main Methods:
- Characterization of the CC-1 repetitive sequence using molecular techniques.
- Hybridization experiments to determine copy numbers and restriction fragment patterns across various rice genomes.
Main Results:
- The CC-1 sequence exhibits variations in repeat unit length (194 bp in CC diploid, 172 bp in BBCC and CCDD tetraploids).
- CC-1 is present in CC, AA, and BB genomes, but absent in EE and FF genomes, with differing copy numbers.
- Significant variations in CC-1 copy numbers and restriction patterns were observed between and within rice species.
Conclusions:
- The CC-1 sequence provides insights into the evolutionary relationships within the rice genus.
- Results suggest the CC genome is more closely related to the AA genome than the BB genome, and distantly related to EE and FF genomes.
More Related Videos
Related Concept Videos
RNA-seq
9.4K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
9.4K
Exon Recombination
3.1K
The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes.
Exon shuffling follows “splice frame rules.” Each exon...
Exon shuffling follows “splice frame rules.” Each exon...
3.1K
DNA-only Transposons
16.0K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
The donor site from where the transposon is excised is either degraded or...
16.0K
Non-LTR Retrotransposons
12.5K
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
12.5K
Chromosome Structure
22.1K
A functional eukaryotic chromosome must contain three elements: a centromere, telomeres, and numerous origins of replication.
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
22.1K
piRNA - Piwi-interacting RNAs
6.1K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
6.1K

