دورية أكاديمية
Protein-DNA interactions define the mechanistic aspects of circle formation and insertion reactions in IS2 transposition
| العنوان: | Protein-DNA interactions define the mechanistic aspects of circle formation and insertion reactions in IS2 transposition |
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| المؤلفون: | Lewis, Leslie A, Astatke, Mekbib, Umekubo, Peter T, Alvi, Shaheen, Saby, Robert, Afrose, Jehan, Oliveira, Pedro H, Monteiro, Gabriel A, Prazeres, Duarte MF |
| المصدر: | Publications and Research |
| بيانات النشر: | CUNY Academic Works |
| سنة النشر: | 2012 |
| المجموعة: | City University of New York: CUNY Academic Works |
| مصطلحات موضوعية: | Curvature propensity plot data, extensive sequence-specific binding, figure-of-eight transposition intermediate, hydroxyl radical footprinting, minicircle junction, selective binding, synaptic complex, transpososome |
| الوصف: | Background Transposition in IS3, IS30, IS21 and IS256 insertion sequence (IS) families utilizes an unconventional two-step pathway. A figure-of-eight intermediate in Step I, from asymmetric single-strand cleavage and joining reactions, is converted into a double-stranded minicircle whose junction (the abutted left and right ends) is the substrate for symmetrical transesterification attacks on target DNA in Step II, suggesting intrinsically different synaptic complexes (SC) for each step. Transposases of these ISs bind poorly to cognate DNA and comparative biophysical analyses of SC I and SC II have proven elusive. We have prepared a native, soluble, active, GFP-tagged fusion derivative of the IS2 transposase that creates fully formed complexes with single-end and minicircle junction (MCJ) substrates and used these successfully in hydroxyl radical footprinting experiments. Results In IS2, Step I reactions are physically and chemically asymmetric; the left imperfect, inverted repeat (IRL), the exclusive recipient end, lacks donor function. In SC I, different protection patterns of the cleavage domains (CDs) of the right imperfect inverted repeat (IRR; extensive in cis) and IRL (selective in trans) at the single active cognate IRR catalytic center (CC) are related to their donor and recipient functions. In SC II, extensive binding of the IRL CD in trans and of the abutted IRR CD in cis at this CC represents the first phase of the complex. An MCJ substrate precleaved at the 3' end of IRR revealed a temporary transition state with the IRL CD disengaged from the protein. We propose that in SC II, sequential 3' cleavages at the bound abutted CDs trigger a conformational change, allowing the IRL CD to complex to its cognate CC, producing the second phase. Corroborating data from enhanced residues and curvature propensity plots suggest that CD to CD interactions in SC I and SC II require IRL to assume a bent structure, to facilitate binding in trans. Conclusions Different transpososomes are assembled in each step of the ... |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| العلاقة: | https://academicworks.cuny.edu/yc_pubs/96Test; https://academicworks.cuny.edu/context/yc_pubs/article/1121/viewcontent/PMC3299598.pdfTest |
| الإتاحة: | https://academicworks.cuny.edu/yc_pubs/96Test https://academicworks.cuny.edu/context/yc_pubs/article/1121/viewcontent/PMC3299598.pdfTest |
| رقم الانضمام: | edsbas.F4B09CB6 |
| قاعدة البيانات: | BASE |
| الوصف غير متاح. |