Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

The activity, divergence, and evolutionary degradation of modern-day homing endonucleases and behavior of their reconstructed ancestors.

Created on 29 Sep 2026

Authors

Juliana C Young, Abigail R Lambert, Janet M Young, Lindsey A Doyle, Miriam Silverstein, David R Edgell, Barry L Stoddard

Published in

Nucleic acids research. Volume 54. Issue 18. Sep 22, 2026.

Abstract

Homing endonucleases (HEs) are selfish genetic elements that drive the mobilization of their own coding sequences, often in concert with surrounding introns. Homing endonuclease genes (HEGs) usually display life cycles in which they accumulate inactivating mutations after invading a host genomic target site, leading to eventual removal from the genome. We identified several hundred novel HEGs and determined the distribution of their proteins' behaviors and activities. Approximately 10% are expressed as well-folded functional proteins that cleave predictable DNA target sites. Another ∼20% display significant expression but little to no cleavage activity; the remainder display severely reduced expression. Despite the presence of debilitating mutations throughout most HEGs, ancestral reconstructions yielded endonucleases with improved expression and stability. One such reconstructed model, at a hypothetical node preceding highly diverged HEs that cleave unique target sites, binds (but does not cleave) their individual targets. It instead cleaves a DNA sequence that resembles a hybrid of those modern-day DNA targets, while displaying a similar specificity profile to previously characterized wild-type HEs. Its DNA-bound crystal structure adds detail to our understanding of how HE DNA contacting surfaces and residues shift and rearrange during evolution, ultimately leading to their action at new target sites.

PMID:
42805603
Bibliographic data and abstract were imported from PubMed on 29 Sep 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 3
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement