Haynes:LitReviewApr2015: Difference between revisions

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==Public Library of Science Biology (PLoS Biology)==
==Public Library of Science Biology (PLoS Biology)==
 
<br> Nothing very relevant. <br>
# Item 1 <br><br>
# (2015) '''Cell Cycle-Dependent Differentiation Dynamics Balances Growth and Endocrine Differentiation in the Pancreas''' Yung Hae Kim, Hjalte List LArsen, Anne Grapin-BOtton, et. al. PLoS Bio. 10.1371:1002111. [http://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.1002111 Link]. <br>'''Summary''': Investigation of differentiation of pancreatic progenitor cells with a focus on differentiating into beta cells for diabetes therapy. Found that endocrine differentiation is largely stochastic. Proposed a model in which the production of a progenitor and a differentiated cell in the pancreas results from the stochastic induction of differentiation in one daughter after cell division, rather than the unequal partitioning of molecules between two daughters at the time of division, as observed in the nervous system<br><br>
# Item 2 <br><br>


==Proceedings of the National Academy of Sciences==
==Proceedings of the National Academy of Sciences==
Line 99: Line 98:
==Science==
==Science==


# Item 1 <br><br>
# (2015) '''Epigenetic inheritance uncoupled from sequence-specific recruitment''' Kaushik Ragunathan, Gloria Jih, and Danesh Moazed. Science. 348:6230. [http://www.sciencemag.org/content/348/6230/1258699.abstract Link]. <br>'''Summary''': Shows that epigenetic inheritable changes in gene expression are not dependent on DNA-specific transcription factors (focuses on H3K9). Constructed a chromatin inducible cell-line similar to the one used in lab.<br><br>
# Item 2 <br><br>
# (2015) '''Combinatorial labeling of single cells for gene expression cytometry''' H. Christina Fan, Glenn K. Fu, Stephen P.A. Fodor. Science. 347:6222. [http://www.sciencemag.org/content/347/6222/1258367.abstract Link]. <br>'''Summary''': New method for gene expression profiling of thousands of single cells across an arbitrary number of genes without using robotics or automation.<br><br>
# (2014) '''Genomically encoded analog memory with precise in vivo DNA writing in living cell populations.''' Fahim Farzadfard and Timothy K. Lu. Science. 346:6211. [http://www.sciencemag.org/content/346/6211/1256272.abstract Link]. <br>'''Summary''': Synthetic Cellular Recorders Integrating Biological Events (SCRIBE) is a new system with uses genomic DNA for analog, rewritable, and flexible memory distributed across living cell populations. SCRIBE enables the recording of analog information such as the magnitude and time span of exposure to an input, SCRIBE-induced mutations can be written and erased and can be used to record multiple inputs across the distributed genomic DNA of bacterial populations. SCRIBE memory can be decomposed into independent input, write, and read operations and used to create genetic logic-and-memory circuits as well as sample-and-hold circuits..<br><br>
'''Review'''
# (2014) '''The new frontier of genome engineering with CRISPR-Cas9''' Jennifer A. Doudna and Emmanuelle Charpentier. Science. 346:6213. [http://www.sciencemag.org/content/346/6213/1258096.abstract Link]. <br>'''Summary''': A good review on using the CRISPR-Cas9 system for genome engineering.<br><br>
 


==Miscellaneous Reviews and Media==
==Miscellaneous Reviews and Media==

Revision as of 18:02, 20 April 2015

<- Back to Publications

JOURNAL ASSIGNMENTS:

  • ACS Synthetic Biology - Rene
  • Cell - Ben
  • Frontiers in Microbiotechnology – David Barclay
  • Journal of Biological Engineering - Ben
  • Journal of Cell Biology - David Tze
  • Molecular Biology of the Cell - David
  • Molecular and Cellular Biology - Rene
  • Nature - Theodore K.
  • Nature Biotechnology - Ryan
  • Nature Methods - Jan
  • Nature Molecular Systems Biology - Ryan
  • Public Library of Science Biology (PLoS Biology) - Cameron
  • Proceedings of the National Academy of Sciences - Jan
  • Science - Cameron
  • Miscellaneous Reviews and Media - Dr. Haynes

INSTRUCTIONS: Please search for lab-relevant articles dated October 2014 up to today.


Spring 2015, 05/21/2015

Use the following text format EXACTLY as it is shown below...

  1. (year) Title. Author One, Author Two, and Author Three et al. Journal. Volume:pages. Link.
    Summary: Very short explanation of why this paper is relevant/ interesting.

  2. (2011) Engineering a Photoactivated Caspase-7 for Rapid Induction of Apoptosis. Evan Mills, Xi Chen, Elizabeth Pham, Stanley Wong, and Kevin Truong et al. ACS Synthetic Biology, 1.3:75-82. Link.
    Summary: A group from University of Toronto developed a protein that causes rapid apotosis (cell death) of targeted cells.

Open edit mode and copy the example above. Do not erase the <br><br> tags!!! Do not use keyboard line returns to space out the numbered list, or else each item will start with the number 1.

ACS Synthetic Biology

  1. Item 1

  2. Item 2

Cell

  1. (2015) Engineering Complex Synthetic Transcriptional Programs with CRISPR RNA Scaffolds. Jesse G. Zalatan, Michael E. Lee, and Ricardo Almeida et al. Cell. 160:339-350. Link.
    Summary: By modifying guide RNAs used in CRISPR to contain sites for recruiting effector proteins, the authors are able to target specific regions of the genome with different actions (such as activation or repression of the gene) mediated through the effector proteins.

  2. (2015) Pioneer Transcription Factors Target Partial DNA Motifs on Nucleosomes to Initiate Reprogramming. Abdenour Soufi, Meilin Fernandez Garcia, and Artur Jaroszewicz et al. Journal. 160:1-14. Link.
    Summary: The 'pioneer' transcription factors are able to recognize sequences partially occluded by nucleosomes. Partial motif recognition occurs through coordinate binding between factors.

Frontiers in Microbiotechnology

  1. Item 1

  2. Item 2

Journal of Biological Engineering

  1. Item 1

  2. Item 2

Journal of Cell Biology

  1. Item 1

  2. Item 2

Molecular Biology of the Cell

  1. Item 1

  2. Item 2

Molecular and Cellular Biology

  1. Item 1

  2. Item 2

Nature

  1. Item 1

  2. Item 2

Nature Biotechnology

  1. Item 1

  2. Item 2

Nature Methods

  1. Item 1

  2. Item 2

Nature Molecular Systems Biology

  1. Item 1

  2. Item 2

Public Library of Science Biology (PLoS Biology)


Nothing very relevant.

  1. (2015) Cell Cycle-Dependent Differentiation Dynamics Balances Growth and Endocrine Differentiation in the Pancreas Yung Hae Kim, Hjalte List LArsen, Anne Grapin-BOtton, et. al. PLoS Bio. 10.1371:1002111. Link.
    Summary: Investigation of differentiation of pancreatic progenitor cells with a focus on differentiating into beta cells for diabetes therapy. Found that endocrine differentiation is largely stochastic. Proposed a model in which the production of a progenitor and a differentiated cell in the pancreas results from the stochastic induction of differentiation in one daughter after cell division, rather than the unequal partitioning of molecules between two daughters at the time of division, as observed in the nervous system

Proceedings of the National Academy of Sciences

  1. Item 1

  2. Item 2

Science

  1. (2015) Epigenetic inheritance uncoupled from sequence-specific recruitment Kaushik Ragunathan, Gloria Jih, and Danesh Moazed. Science. 348:6230. Link.
    Summary: Shows that epigenetic inheritable changes in gene expression are not dependent on DNA-specific transcription factors (focuses on H3K9). Constructed a chromatin inducible cell-line similar to the one used in lab.

  2. (2015) Combinatorial labeling of single cells for gene expression cytometry H. Christina Fan, Glenn K. Fu, Stephen P.A. Fodor. Science. 347:6222. Link.
    Summary: New method for gene expression profiling of thousands of single cells across an arbitrary number of genes without using robotics or automation.

  3. (2014) Genomically encoded analog memory with precise in vivo DNA writing in living cell populations. Fahim Farzadfard and Timothy K. Lu. Science. 346:6211. Link.
    Summary: Synthetic Cellular Recorders Integrating Biological Events (SCRIBE) is a new system with uses genomic DNA for analog, rewritable, and flexible memory distributed across living cell populations. SCRIBE enables the recording of analog information such as the magnitude and time span of exposure to an input, SCRIBE-induced mutations can be written and erased and can be used to record multiple inputs across the distributed genomic DNA of bacterial populations. SCRIBE memory can be decomposed into independent input, write, and read operations and used to create genetic logic-and-memory circuits as well as sample-and-hold circuits..

Review

  1. (2014) The new frontier of genome engineering with CRISPR-Cas9 Jennifer A. Doudna and Emmanuelle Charpentier. Science. 346:6213. Link.
    Summary: A good review on using the CRISPR-Cas9 system for genome engineering.


Miscellaneous Reviews and Media

Reviews

  1. Item 1

  2. Item 2

News

  1. Item 1

  2. Item 2