Consensus sequence

Consensus sequence is a sequence of DNA or RNA that is similar or identical between different molecules or within a single molecule. It is a way of representing the results of sequence alignment where multiple sequences are compared and the similarities between them are determined.

Overview[edit | edit source]

A consensus sequence is derived from the most frequent residues found at each position in a sequence alignment. They are used in sequence logos to visually represent patterns and frequencies of nucleotide or amino acid sequences.

Consensus sequences are important in the fields of molecular biology and genetics because they can highlight regions of similarity and difference. They are often used to infer functional, structural, or evolutionary relationships between sequences.

Role in Molecular Biology[edit | edit source]

In molecular biology, consensus sequences are used to predict the presence and location of genetic elements, such as promoters, enhancers, and splice sites. These sequences are often found in the regulatory regions of genes and can be critical for the proper expression of those genes.

For example, the TATA box is a consensus sequence that is found in the promoter region of many genes in eukaryotes. It is recognized and bound by the TATA-binding protein, which is part of the transcription factor complex that initiates transcription.

Role in Genetics[edit | edit source]

In genetics, consensus sequences can be used to identify potential genetic variation and to predict the effects of mutations. For instance, a mutation that changes a consensus sequence might disrupt the normal function of a gene, leading to a genetic disorder.

References[edit | edit source]

Consensus sequence Resources
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