Neighboring inteins interfere with one another's homing capacity

Author:

Turgeman-Grott Israela1,Arsenault Danielle2,Yahav Dekel1,Feng Yutian2ORCID,Miezner Guy1,Naki Doron1,Peri Omri1,Papke R Thane2,Gogarten Johann Peter23ORCID,Gophna Uri1

Affiliation:

1. The Shmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University , P.O. Box 39040, 6997801 Tel Aviv , Israel

2. Department of Molecular and Cell Biology, University of Connecticut , 91 North Eagleville Road, Storrs, CT 06268-3125 , USA

3. Institute for Systems Genomics, University of Connecticut , 67 North Eagleville Road, Storrs, CT 06268-3003 , USA

Abstract

Abstract Inteins are mobile genetic elements that invade conserved genes across all domains of life and viruses. In some instances, a single gene will have several intein insertion sites. In Haloarchaea, the minichromosome maintenance (MCM) protein at the core of replicative DNA helicase contains four intein insertion sites within close proximity, where two of these sites (MCM-a and MCM-d) are more likely to be invaded. A haloarchaeon that harbors both MCM-a and MCM-d inteins, Haloferax mediterranei, was studied in vivo to determine intein invasion dynamics and the interactions between neighboring inteins. Additionally, invasion frequencies and the conservation of insertion site sequences in 129 Haloferacales mcm homologs were analyzed to assess intein distribution across the order. We show that the inteins at MCM-a and MCM-d recognize and cleave their respective target sites and, in the event that only one empty intein invasion site is present, readily initiate homing (i.e. single homing). However, when two inteins are present co-homing into an intein-free target sequence is much less effective. The two inteins are more effective when invading alleles that already contain an intein at one of the two sites. Our in vivo and computational studies also support that having a proline in place of a serine as the first C-terminal extein residue of the MCM-d insertion site prevents successful intein splicing, but does not stop recognition of the insertion site by the intein's homing endonuclease.

Funder

National Science Foundation

NSF

MCB

European Research Council

Publisher

Oxford University Press (OUP)

Reference50 articles.

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