Palindromic sequence should not be confused with inverted repeat.
A palindromic sequence is a nucleic acid sequence in a double-stranded DNA or RNA molecule whereby reading in a certain direction (e.g. 5' to 3') on one strand is identical to the sequence in the same direction (e.g. 5' to 3') on the complementary strand. This definition of palindrome thus depends on complementary strands being palindromic of each other.
The meaning of palindrome in the context of genetics is slightly different from the definition used for words and sentences. Since a double helix is formed by two paired antiparallel strands of nucleotides that run in opposite directions, and the nucleotides always pair in the same way (adenine (A) with thymine (T) in DNA or uracil (U) in RNA; cytosine (C) with guanine (G)), a (single-stranded) nucleotide sequence is said to be a palindrome if it is equal to its reverse complement. For example, the DNA sequence ACCTAGGT is palindromic with its nucleotide-by-nucleotide complement TGGATCCA because reversing the order of the nucleotides in the complement gives the original sequence.
A palindromic nucleotide sequence is capable of forming a hairpin. The stem portion of the hairpin is a pseudo-double stranded portion since the entire hairpin is a part of same (single) strand of nucleic acid. Palindromic motifs are found in most genomes or sets of genetic instructions. They have been specially researched in bacterial chromosomes and in the so-called Bacterial Interspersed Mosaic Elements (BIMEs) scattered over them. In 2008, a genome sequencing project discovered that large portions of the human X and Y chromosomes are arranged as palindromes.[1] A palindromic structure allows the Y chromosome to repair itself by bending over at the middle if one side is damaged.
Palindromes also appear to be found frequently in the peptide sequences that make up proteins,[2] [3] but their role in protein function is not clearly known. It has been suggested that the existence of palindromes in peptides might be related to the prevalence of low-complexity regions in proteins, as palindromes are frequently associated with low-complexity sequences. Their prevalence may also be related to the propensity of such sequences to form alpha helices[4] or protein/protein complexes.[5]
Palindromic sequences play an important role in molecular biology. Because a DNA sequence is double stranded, the base pairs are read, (not just the bases on one strand), to determine a palindrome. Many restriction endonucleases (restriction enzymes) recognize specific palindromic sequences and cut them. The restriction enzyme EcoR1 recognizes the following palindromic sequence:
5'- G A A T T C -3' 3'- C T T A A G -5'
The top strand reads 5'-GAATTC-3', while the bottom strand reads 3'-CTTAAG-5'. If the DNA strand is flipped over, the sequences are exactly the same (5'GAATTC-3' and 3'-CTTAAG-5'). Here are more restriction enzymes and the palindromic sequences which they recognize:
| Enzyme | Source | Recognition Sequence | Cut | |
|---|---|---|---|---|
| EcoR1 | Escherichia coli | 5'GAATTC 3'CTTAAG | 5'---G AATTC---3' 3'---CTTAA G---5' | |
| BamH1 | Bacillus amyloliquefaciens | 5'GGATCC 3'CCTAGG | 5'---G GATCC---3' 3'---CCTAG G---5' | |
| Taq1 | Thermus aquaticus | 5'TCGA 3'AGCT | 5'---T CGA---3' 3'---AGC T---5' | |
| Alu1 | Arthrobacter luteus | 5'AGCT 3'TCGA | 5'---AG CT---3' 3'---TC GA---5' | |
Palindromic sequences may also have methylation sites.These are the sites where a methyl group can be attached to the palindromic sequence. Methylation makes the resultant gene inactive; this is called insertional inactivation or insertional mutagenesis. For example, in PBR322 methylation at the tetracyclin resistant gene makes the plasmid liable to tetracyclin; after methylation at the tetracyclin resistant gene if the plasmid is exposed to antibiotic tetracyclin, it does not survive.
Diversity of T cell receptor (TCR) genes is generated by nucleotide insertions upon V(D)J recombination from their germline-encoded V, D and J segments. Nucleotide insertions at V-D and D-J junctions are random, but some small subsets of these insertions are exceptional, in that one to three base pairs inversely repeat the sequence of the germline DNA. These short complementary palindromic sequences are called P nucleotides.[6]