Overview and logistics
In Module 1, you delivered a mini-presentation that was focused on your research project. For this assignment, you will present work completed by other scientists that has been peer-reviewed and published. Reading, understanding, and explaining research related to your project are all important skills that will be important as you flex your scientist muscles.
As you prepare your talk be sure to follow the specific guidelines for oral presentations in this class.
Also, please use the following link to view the full video from Susan McConnell: Designing effective scientific presentations
You will complete this assignment individually.
Selecting an article to present
You may choose to select a journal article from those provided by the teaching faculty or you can select an article that is related to your Module 2 research from any peer-reviewed journal.
- If you choose an article from below, please "reserve" it by putting your (initials/lab section/team color) next to the listing here.
- For visibility, please use the following format to sign up if possible, substituting in your own initials and team color: <font color = purple><b>[ANS/WF/Purple]</b></font color>, which will look like [ANS/WF/Purple]. Thanks!
- If you would like to discuss a paper not on the list below, please email it (as .pdf) to your instructor with a brief description of the work.
- The list of papers below is provided as a guideline for the types of papers that might be relevant for your presentation. You are not limited to the primary research articles on this list. The list is provided simply to give you an idea of the kinds of subjects that could make suitable presentations for the class. Feel free to search PubMed yourself to find articles of interest to you.
- The same paper may be presented by a T/R and a W/F student, but may only be presented once per section.
Method of submission
Please submit your completed slides on Stellar, with filename Name_LabSection_Mod2JC.doc (for example, LeonaSamson_TR_Mod2JC.pptx).
Your journal club slides are due by 1 pm on the day of your presentation.
- The choice of presentation order will be given to students who submitted their slides earliest.
Length and location of presentations
You will have 10 minutes to discuss the journal article you select. It may be very difficult, or impossible, to discuss all of the figures within the article adequately in only 10 minutes. Therefore, this assignment is not only to present the work, but also to identify the data that is most important to the conclusions. It is also critical to consider how your presentation 'flows' from one experiment to the next. As when you write your own research, you want to deliver a coherent story during your journal presentation.
On both journal club presentation days, we will meet in 16-336 and begin at 1:05 pm sharp. Presenters should arrive early and will be able to check their slides on the large screen.
Journal article options
If the links below do not work, the easiest way to locate each paper is to type the "PMID" (PubMed identifier) in at the PubMed website. If that approach gives you an error for some reason, or in future cases where you might not know the PMID, you can try typing the title of your article into PubMed to find it. If you have trouble accessing your article directly from there, go to http://libraries.mit.edu/vera, which is MIT's collection of journals online. Try selecting "exact title" from the search pulldown menu if the name of your journal is a common word such as Science. For older articles, you need to choose the JSTOR rather than Highwire interface.
- Ahmed, E. A. et al. DNA double strand break response and limited repair capacity in mouse elongated spermatids. (2015) Int J Mol Sci. PMID:26694360 [NEK/TR/Green] [AMG/WF/Pink]
- Banerjee, R. et al. TRIP13 promotes error-prone nonhomologous end joining and induces chemoresistance in head and neck cancer. (2014) Nat Comm. PMID:25078033 [HS/TR/Orange][AH/WF/Red]
- Chang, H-Y. et al. RON nuclear translocation under hypoxia potentiates chemoresistance to DNA double-strand break-inducing anticancer drugs. (2016) Mol Cancer Ther. PMID:26772202[NZ/TR/Pink][MAS/WF/Blue]
- Chang, C-F. et al. PHRF1 promotes genome integrity by modulating non-homologous end-joining. (2015) PMID:25855964
- Chen, P. et al. Thrombospondin-1 might be a therapeutic target to suppress RB cells by regulating the DNA double-strand breaks repair. (2016) PMID:26756218 [JS/TR/Green]
- Gelot, C. et al. The cohesin complex prevents the end joining of distant DNA double-strand ends. (2016) Mol Cell. PMID:26687679 [CD/TR/Blue]
- Goglia, A. G. et al. Identification of novel radiosensitizers in a high-throughput, cell-based screen for DSB repair inhibitors. (2014) Mol Cancer Ther. PMID:25512618[RVP/WF/Blue][RA/TR/Yellow]
- Ismail, I. H. et al. The RNF138 E3 ligase displaces Ku to promote DNA end resection and regulate DNA repair pathway choice. (2014) Nat Cell Biol. PMID:26502055 [JS/WF/Orange][ES/TR/Pink]
- Kraft, D. et al. NF-KB-dependent DNA damage-signaling differentially regulates DNA double-strand break repair mechanisms in immature and mature human hematopoietic cells. (2015) Leukemia. [EB/TR/Yellow]PMID:25652738
- Lee, K-J. et al. Phosphorylation of Ku dictates DNA double-strand break (DSB) repair pathway choice in S phase. (2015) Nuc Acids Res. PMID:26712563 [OMG/TR/Red] [YA/WF/Purple]
- Liang, Z. et al. Overhang polarity of chromosomal double-strand breaks impacts kinetics and fidelity of yeast non-homologous end joining. (2016) Nuc Acids Res. PMID:26773053
- Maggio, I. et al. Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations. (2016) Nuc Acids Res. PMID:26762977
- Marampon, F. et al. Cyclin D1 silencing suppresses tumerigenicity, impairs DNA double strand break repair and thus radiosensitizes androgen-independent prostrate cancer cells to DNA damage. (2015) Oncotarget. PMID:26689991 [PB/WF/Blue]
- Ren, C. et al. Dual-reporter surrogate systems for efficient enrichment of genetically modified cells. (2015) Cell Mol Life Sci. PMID:25725802 [NO/TR/Orange]
- Suzuki, A. et al. Gene expression analysis using strains constructed by NHEJ-mediated one-step promoter cloning in the yeast Kluymeromyces marxianus. (2015) FEMS Yeast Res. PMID:26136515
- Wang, G. et al. CRISPR-Cas9 can inhibit HIV-1 replication but NHEJ repair facilitates virus escape. (2016) Mol Therapy. PMID:26796669 [BNB/TR/Red] [AL/WF/Red]
- Zhang, Q. et al. FBXW7 facilitates nonhomologous end-joining via K63-linked polyubiquitylation of XRCC4. (2016) Mol Cell. PMID:26774286
- Zhang, W. et al. SIRT1 inhibition impairs non-homologous end joining DNA damage repair by increasing Ku70 acetylation in chronic myeloid leukemia cells. (2015) Oncotarget. PMID:26646449 [PL/TR/Blue] [GL/WF/Purple]
- Zhu, L. et al. CRISPR/Cas9-mediated knockout of factors in hon-homologous end joining pathway enhances gene targeting in silkworm cells. (2015) Nat Sci Reports. PMID:26657947 [SS/TR/Purple] [SRH/WF/Pink]
Presentation day reservation
Please put your name under the day you wish to present. There are up to 7 slots on each day. Slot location does not determine speaker order.
||Day 4 (T/R)
||Day 8 (T/R)
||Day 4 (W/F)
||Day 8 (W/F)
||Alexa M Garcia
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