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Homing endonucleases

LAGLIDADG endonuclease
PDB 1p8k EBI.jpg
the structure and dna recognition of a bifunctional homing endonuclease and group i intron splicing factor
Identifiers
Symbol LAGLIDADG_1
Pfam PF00961
Pfam clan CL0324
InterPro IPR001982
SCOP 1af5
SUPERFAMILY 1af5
LAGLIDADG DNA endonuclease family
PDB 1r7m EBI.jpg
the homing endonuclease i-scei bound to its dna recognition region
Identifiers
Symbol LAGLIDADG_2
Pfam PF03161
Pfam clan CL0324
InterPro IPR004860
Homing endonuclease
PDB 1ef0 EBI.jpg
crystal structure of pi-scei miniprecursor
Identifiers
Symbol Hom_end
Pfam PF05204
Pfam clan CL0324
InterPro IPR007869
SCOP 1gpp
SUPERFAMILY 1gpp
Hom_end-associated Hint
PDB 1ef0 EBI.jpg
crystal structure of pi-scei miniprecursor
Identifiers
Symbol Hom_end_hint
Pfam PF05203
Pfam clan CL0363
InterPro IPR007868
SCOP 1gpp
SUPERFAMILY 1gpp

The homing endonucleases are a collection of endonucleases encoded either as freestanding genes within introns, as fusions with host proteins, or as self-splicing inteins. They catalyze the hydrolysis of genomic DNA within the cells that synthesize them, but do so at very few, or even singular, locations. Repair of the hydrolyzed DNA by the host cell frequently results in the gene encoding the homing endonuclease having been copied into the cleavage site, hence the term 'homing' to describe the movement of these genes. Homing endonucleases can thereby transmit their genes horizontally within a host population, increasing their allele frequency at greater than Mendelian rates.

Although the origin and function of homing endonucleases is still being researched, the most established hypothesis considers them as selfish genetic elements, similar to transposons, because they facilitate the perpetuation of the genetic elements that encode them independent of providing a functional attribute to the host organism.

Homing endonuclease recognition sequences are long enough to occur randomly only with a very low probability (approximately once every 7×109 bp), and are normally found in one or very few instances per genome. Generally, owing to the homing mechanism, the gene encoding the endonuclease (the HEG, "homing endonuclease gene") is located within the recognition sequence which the enzyme cuts, thus interrupting the homing endonuclease recognition sequence and limiting DNA cutting only to sites that do not (yet) carry the HEG.

Prior to transmission, one allele carries the gene (HEG+) while the other does not (HEG), and is therefore susceptible to being cut by the enzyme. Once the enzyme is synthesized, it breaks the chromosome in the HEG allele, initiating a response from the cellular DNA repair system. The damage is repaired using recombination, taking the pattern of the opposite, undamaged DNA allele, HEG+, that contains the gene for the endonuclease. Thus, the gene is copied to the allele that initially did not have it and it is propagated through successive generations. This process is called "homing".


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