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      A load driver device for engineering modularity in biological networks

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          Abstract

          The behavior of gene modules in complex synthetic circuits is often unpredictable 14 . Upon joining modules to create a circuit, downstream elements (such as binding sites for a regulatory protein) apply a load to upstream modules that can negatively affect circuit function 1, 5 . Here we devise a genetic device named a load driver that mitigates the impact of load on circuit function, and we demonstrate its behavior in Saccharomyces cerevisiae. The load driver implements the design principle of time scale separation: inclusion of the load driver’s fast phosphotransfer processes restores the capability of a slower transcriptional circuit to respond to time-varying input signals even in the presence of substantial load. Without the load driver, we observe circuit behavior that suffers from 76% delay in response time and a 25% decrease in system bandwidth due to load. With the addition of a load driver, circuit performance is almost completely restored. Load drivers will serve as fundamental building blocks in the creation of complex, higher level genetic circuits.

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          Most cited references54

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          Improved method for high efficiency transformation of intact yeast cells.

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            Foundations for engineering biology.

            Drew Endy (2005)
            Engineered biological systems have been used to manipulate information, construct materials, process chemicals, produce energy, provide food, and help maintain or enhance human health and our environment. Unfortunately, our ability to quickly and reliably engineer biological systems that behave as expected remains quite limited. Foundational technologies that make routine the engineering of biology are needed. Vibrant, open research communities and strategic leadership are necessary to ensure that the development and application of biological technologies remains overwhelmingly constructive.
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              A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast.

              Heterologous markers are important tools required for the molecular dissection of gene function in many organisms, including Saccharomyces cerevisiae. Moreover, the presence of gene families and isoenzymes often makes it necessary to delete more than one gene. We recently introduced a new and efficient gene disruption cassette for repeated use in budding yeast, which combines the heterologous dominant kan(r) resistance marker with a Cre/loxP-mediated marker removal procedure. Here we describe an additional set of four completely heterologous loxP-flanked marker cassettes carrying the genes URA3 and LEU2 from Kluyveromyces lactis, his5(+) from Schizosaccharomyces pombe and the dominant resistance marker ble(r) from the bacterial transposon Tn5, which confers resistance to the antibiotic phleomycin. All five loxP--marker gene--loxP gene disruption cassettes can be generated using the same pair of oligonucleotides and all can be used for gene disruption with high efficiency. For marker rescue we have created three additional Cre expression vectors carrying HIS3, TRP1 or ble(r) as the yeast selection marker. The set of disruption cassettes and Cre expression plasmids described here represents a significant further development of the marker rescue system, which is ideally suited to functional analysis of the yeast genome.
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                Author and article information

                Journal
                9604648
                20305
                Nat Biotechnol
                Nat. Biotechnol.
                Nature biotechnology
                1087-0156
                1546-1696
                6 September 2014
                24 November 2014
                December 2014
                01 June 2015
                : 32
                : 12
                : 1268-1275
                Affiliations
                [1 ]Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA
                [2 ]Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, MA, USA
                [3 ]Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA
                [4 ]Laboratory for Information and Decision Systems, Massachusetts Institute of Technology, Cambridge, MA, USA
                [5 ]Department of Electrical Engineering/Computer Science, Massachusetts Institute of Technology, Cambridge, MA, USA
                Author notes
                [* ]Correspondence to: rweiss@ 123456mit.edu (R.W.) and ddv@ 123456mit.edu (D.D.V.)
                Article
                NIHMS625853
                10.1038/nbt.3044
                4262674
                25419739
                c8d25099-b413-4020-b5ab-a49098be599e
                History
                Categories
                Article

                Biotechnology
                Biotechnology

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