کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2184343 1095831 2016 18 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Brujita Integrase: A Simple, Arm-Less, Directionless, and Promiscuous Tyrosine Integrase System
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Brujita Integrase: A Simple, Arm-Less, Directionless, and Promiscuous Tyrosine Integrase System
چکیده انگلیسی


• Phage Brujita integrase is a non-canonical tyrosine integrase.
• Integration/excision is promiscuous in site selection and lacks directional control.
• Integration requires simple attachment sites with only core-type Integrase binding sites.
• Integrase binding to attP and attB requires unusual cooperative interactions.
• A simple recombinase for phage integration may be ancestral to complex integration systems.

Mycobacteriophage Brujita is an unusual temperate phage in which establishment of superinfection immunity is dependent on chromosomal integration. Integration is mediated by a non-canonical tyrosine integrase (Int) lacking an N-terminal domain typically associated with binding to arm-type sites within the phage attachment site (attP). This raises the question as to how these Ints bind their DNA substrates, if they form higher-order protein DNA complexes, and how site selection and recombinational directionality are determined. Here we show that Brujita Int is a simple recombinase, whose properties more closely resemble those of FLP and Cre than it does the canonical phage Ints. Brujita Int uses relatively small DNA substrates, fails to discriminate between attP and attB, cleaves attachment site DNA to form a 6-base overlap region, and lacks directional control. Brujita Int also has an unusual pattern of binding to its DNA substrates. It binds to two half sites (B and B′) at attB, although binding to the B half site is strongly dependent on occupancy of B′. In contrast, binding to the P half site is not observed, even when Int is bound at P′. However, an additional Int binding site (P1) is displaced to the left of the crossover site at attP, is required for recombination and is predicted to facilitate binding of Int to the P half site during synapsis. These simple phage Int systems may reflect ancestral states of phage evolution with the complexities of higher-order complex formation and directional control representing subsequent adaptations.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Biology - Volume 428, Issue 11, 5 June 2016, Pages 2289–2306
نویسندگان
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