Difference between revisions of "Papers of the month"

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=2013=
 
=2013=
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* '''May 2013'''
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** [http://www.ncbi.nlm.nih.gov/pubmed/23538833 Paul et al.] demonstrate that the orientation of the genes on the chromosome has a significant impact on their evolution: Gene encoded on the lagging strand evolve faster than those on the leading strand. This faster evolution is caused by collisions between the [[DNA replication]] and [[transcription]] machineries that result in DNA damage and subsequent fixation of errors as mutations. Importantly, [[essential genes]] are strongly underrepresented on the lagging strand thus providing a "built-in" protection of the encoded important proteins against possible deleterious mutations.
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** '''Relevant ''Subti''Wiki pages:'''  [[transcription]], [[DNA replication]], [[essential genes]]
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<pubmed> 23538833 </pubmed>
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* '''April 2013'''
 
* '''April 2013'''
 
** Usually, [[cell wall synthesis]] is regarded as being essential for ''B. subtilis''. Now, [http://www.ncbi.nlm.nih.gov/pubmed/23452849 Mercier et al.] from the lab of [[Jeff Errington]] show that excess biosynthesis of membranes is sufficient to drive the formation of cell wall-less L-forms in B. subtilis. Interestingly, this cell form is even independent of the essential [[cell division]] protein [[FtsZ]].
 
** Usually, [[cell wall synthesis]] is regarded as being essential for ''B. subtilis''. Now, [http://www.ncbi.nlm.nih.gov/pubmed/23452849 Mercier et al.] from the lab of [[Jeff Errington]] show that excess biosynthesis of membranes is sufficient to drive the formation of cell wall-less L-forms in B. subtilis. Interestingly, this cell form is even independent of the essential [[cell division]] protein [[FtsZ]].

Revision as of 10:00, 1 May 2013

2013

  • May 2013
    • Paul et al. demonstrate that the orientation of the genes on the chromosome has a significant impact on their evolution: Gene encoded on the lagging strand evolve faster than those on the leading strand. This faster evolution is caused by collisions between the DNA replication and transcription machineries that result in DNA damage and subsequent fixation of errors as mutations. Importantly, essential genes are strongly underrepresented on the lagging strand thus providing a "built-in" protection of the encoded important proteins against possible deleterious mutations.
    • Relevant SubtiWiki pages: transcription, DNA replication, essential genes



  • March 2013
    • The mechanism of membrane fission in bacteria has been a long-standing enigma. Now, Doan et al. from the lab of David Rudner demonstrate how the FisB protein (previously YunB) mediates membrane fission during sporulation This activity of FisB is based on its ability to bind to lipids, specifically to cardiolipin.
    • Relevant SubtiWiki pages: David Rudner, FisB, sporulation

  • See also:


  • A comment on this paper:

  • See also:



2012

  • December 2012
    • Kim et al.. show how the ATP hydrolysis controls the global conformation of the SecA translocase and drives protein secretion. The intricate network of structural interactions, which couple local electrostatic changes during ATP hydrolysis to global conformational and dynamic changes in SecA, form the foundation of the allosteric mechanochemistry that efficiently harnesses the chemical energy stored in ATP to drive complex mechanical processes.
    • Relevant SubtiWiki pages: SecA, protein secretion









Levdikov VM, Blagova EV, McFeat A, Fogg MJ, Wilson KS, Wilkinson AJ  
Structure of components of an intercellular channel complex in sporulating Bacillus subtilis. 
Proc Natl Acad Sci U S A. 2012, 109(14):5441-5. 
PubMed:22431604


  • A comment on these papers:


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2011


Locke JC, Young JW, Fontes M, Hernández Jiménez MJ, Elowitz MB  
Stochastic pulse regulation in bacterial stress response. 
Science. 2011 334:366-369. 
PubMed:21979936



Lehnik-Habrink M, Schaffer M, Mäder U, Diethmaier C, Herzberg C, Stülke J  
RNA processing in Bacillus subtilis: identification of targets of the essential RNase Y. 
Mol Microbiol. 2011 81(6): 1459-73. 
PubMed:21815947



  • A comment on these papers:



  • May 2011
    • Miles et al. identified the enzyme for the key final step in the biosynthesis of queuosine, a hypermodified base found in the wobble positions of tRNA Asp, Asn, His, and Tyr from bacteria to man
    • Relevant SubtiWiki pages: QueG, translation