Exact word matches in rice pseudomolecules.
Shaolin Liu1, Nicholas A Tinker, Diane E Mather
1Department of Plant Science, McGill University, Ste-Anne-de-Bellevue, Canada.
Genome
|October 13, 2006
Summary
Rice genomes show non-random usage of short DNA sequences ("words"). Frequently repeated words within the rice genome are often unique to rice, suggesting genomic specificity.
Area of Science:
- Genomics
- Bioinformatics
Background:
- Understanding genome organization and sequence usage is crucial for deciphering gene regulation and evolutionary history.
- Oligonucleotide (oligo) frequencies can reveal patterns of sequence selection and constraint within genomes.
Purpose of the Study:
- To analyze the frequencies of oligonucleotide "words" across the rice genome (Oryza sativa L. subsp. japonica).
- To investigate the distribution and uniqueness of these sequence words within the rice genome and their potential association with genomic features.
Main Methods:
- Computation of frequencies for 6 to 24 bp oligos across the assembled rice genome.
- Annotation of nucleotide positions with genome-wide frequencies of 18 bp oligos.
- BLASTn searches to assess the species-specificity of high-frequency oligos.
Main Results:
- All oligos ≤10 bp were repeated at least 12 times; unique oligo percentage increased with length (0.1% for 12 bp to 76.0% for 24 bp).
- Oligo frequencies formed landscapes with high- and low-frequency zones; low-frequency zones had high-frequency spikes potentially linked to RIM2 transposon activity.
- High-frequency non-SSR 18 bp oligos were largely unique to rice, indicating sequence specificity.
Conclusions:
- Oligonucleotide word usage is non-random across different regions within the rice genome.
- Frequently repeated sequence words within the rice genome tend to be species-specific, suggesting evolutionary constraints or selection.
Related Concept Videos
¹H NMR: Pople Notation
The Pople nomenclature system classifies spin systems based on the difference between their chemical shifts. Coupled spins are denoted by capital letters with subscripts indicating the number of equivalent nuclei. When the coupled nuclei have well-separated chemical shifts, they are assigned letters that are far apart in the alphabet, such as A and X. When the difference in chemical shifts is small, coupled nuclei are named using adjacent letters of the alphabet (AB, MN, or XY).
A proton...
A proton...
Riboswitches
Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
¹H NMR Chemical Shift Equivalence: Homotopic and Heterotopic Protons
Protons in identical electronic environments within a molecule are chemically equivalent and have the same chemical shift. The replacement test is a useful tool to identify chemical equivalence and predict NMR spectra. A substituent replaces each of the protons being examined and the resulting molecules are compared. If the same molecule is obtained, the protons are equivalent or homotopic. Replacement of any hydrogens in ethane by chlorine yields chloroethane because all six protons are...
Isomerism
Isomers are molecules with the same molecular formula but different structural arrangements. Isomers can be further classified into constitutional isomers and stereoisomers. Constitutional isomers differ in the connectivity of their constituent atoms. For example, 2-butanol and diethyl ether are constitutional isomers, as they have the same chemical formula, C4H10O, but differ in the connectivity of the carbon and oxygen atoms. Constitutional isomers have different physical and chemical...
Polymer Classification: Crystallinity
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Chirality at Nitrogen, Phosphorus, and Sulfur
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...


