Difference between revisions of "Team:HZAU-China/Project/Description"

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    <img src="https://static.igem.org/mediawiki/2017/8/8e/HZAU_2017_background_1.png" class="beijin">
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     <div style="height:80000px;">content</div>
    <ul class="daohang">
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      <li id="HZAU_menu_1">
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        <a href="#" id="bianse_1">Background</a>
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      </li>
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      <li id="HZAU_menu_2">
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        <a href="#item2_1" id="bianse_2">Information</a>
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      </li>
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      <li id="HZAU_menu_3">
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        <a href="#item3_1" id="bianse_3">Why light control</a>
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  <div class="HZAU_content wrap">
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    <div class="item" id="item1">
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      <a class="biaoti">Description</a>
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      <a class="zhengwen">In the long history of life evolution, different species living in different environment developed the most adaptive
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        surviving mechanism for them under the selection pressure, among which some unmatchable become widly preserved in
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        different creatures, and the mechanism of replication is one of them. The majority of prokaryote share the same mechanism
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        of self-replication including DNA replication, chromosome seperation and cell division. These three parts comprised
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        the whole cell cycle, and the main model creature for researching the replication process is E.coli, which at the
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        same time is the main object of our project.</a>
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    </div>
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    <img src="https://static.igem.org/mediawiki/2017/b/bc/HZAU_2017_tu1_1.png" class="tu_1">
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    <div class="item" id="item2">
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        <div id="item2_1" class="zhengwen"></div>
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      <a class="zhengwen">The replication process of E.coli replication can be devided into phase B,C and D, three phases. Phase B, also called
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        pre-replication phase, is for DNA replication proparation similar as G1 phase in eukaryote cell cycle. Phase C is
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        regarded as replication phase during which the chromosome is replicating corespond to the S phase in eukaryote. The
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        last phase, phase D, is called post-replication phase, in which the behave of chromosome seperation and cell division
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        happend just like what happened in G2 and M phase of eukaryote cells. the time of C phase and D phase in a generation
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        is relative constant, so what actually determines the cell cycle is the initiation of genome replication. We know
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        that cell have to garantee that each cell should have at least one chormosome, and this requires a highly coordination
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        between DNA replication and cell divsion. Though the delicate mechanism of the corrdination is still a puzzle, it
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        is clear that DnaA protein plays a significant role in this event. DnaA is a versatile protein, it can not only behave
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        like a helicase opening the duble-helix of replication initiation site, OriC, while have the function of raising
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        other proteins forming into the replisome to prolong the replication, but also can anchor the replicationg choromosome
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        on the cell membrane leading the following seperation of chromosome. But what makes it the linker between replication
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        and division is that its concentration determines the initiation volume of replication. So according to these information,
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        we think that regulating the combination of DNA and DnaA protein will be an efficient method to regulate cell replication.
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        <a href="">For more information please click here.</a>
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      </a>
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     </div>
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    <div class="item" id="item3">
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      <div id="item3_1" class="zhengwen"></div>
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      <a class="zhengwen">There will be about 1h for an entire genome replication, but cell division can reach about 20min per generation. this
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        reflects the multi-copy number of bacterial genome and only with this mechanism can E.coli reproduce in such a high
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        speed. what's worse is that even isogenic cells grow in the same culture have a scattering distribution not only
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        in phase but also in genome copy number. the strong heterogenic in cell cycle and genome copy number hinds the 3D
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        genome research and may be a potential noise on genome gene expression. At the same time, the developing synthetic
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        biology requires an approach that can control cell reproduction and can be easily incorporated into circuits, so
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        that the whole system can be more safe and controlable. taking these into consider, we decided to use CRISPRi to
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        inhibit its cell cycle, for more details please see design.</a>
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      <a class="zhengwen">But barely pause the replication in some circumstance can't satisfy our needs, and long time inhibition will prolong
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        its length, so there is a need to totally control its replication, not only block but also open. with that purpose
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        we decided to use optogentic to control this system, and the operablity of light to computer makes our system programable,
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        which can be called 4C.</a>
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    </div>
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    <a class="ppp"></a>
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Revision as of 14:56, 27 October 2017

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