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<title>Journal of Molecular Cell Biology - current issue</title>
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<description>Journal of Molecular Cell Biology - RSS feed of current issue</description>
<prism:coverDisplayDate>December 2009</prism:coverDisplayDate>
<prism:publicationName>Journal of Molecular Cell Biology</prism:publicationName>
<prism:issn>1674-2788</prism:issn>
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<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/55?rss=1">
<title><![CDATA[Macrophage Metalloelastase: Stretching Therapeutic Opportunities]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/55?rss=1</link>
<description><![CDATA[
<p>While tissue macrophages are at the first line of microbial host defense, they are also convenient hideouts for pathogens escaping immune attack. Houghton et al. discovered that alveolar macrophage mobilizes macrophage metalloelastase to destroy bacteria present inside the cell.</p>
]]></description>
<dc:creator><![CDATA[He, J. Q., van Lookeren Campagne, M.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp015</dc:identifier>
<dc:title><![CDATA[Macrophage Metalloelastase: Stretching Therapeutic Opportunities]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>57</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>55</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/58?rss=1">
<title><![CDATA[Cohesin: A Multi-purpose Chromatin Glue]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/58?rss=1</link>
<description><![CDATA[
<p>Long thought to be the glue responsible for holding sister chromatids together, cohesin has been found to be stickier than previously thought. Recent discoveries point to cohesin having a role in transcription regulation by mediating long-distance intra-chromosomal interactions.</p>
]]></description>
<dc:creator><![CDATA[Diaz-Martinez, L. A., Yu, H.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp014</dc:identifier>
<dc:title><![CDATA[Cohesin: A Multi-purpose Chromatin Glue]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>60</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>58</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/61?rss=1">
<title><![CDATA[Dynamic Balancing: DEPTOR Tips the Scales]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/61?rss=1</link>
<description><![CDATA[
<p>The mammalian target of rapamycin, mTOR, is a key node in cellular regulation: its dysregulation is important in a number of disease states, including various cancers. A recent study identifies a new partner and regulator of mTOR, which can alter the balance of signaling downstream of mTOR and appears to be important in certain cancers, such as multiple myelomas.</p>
]]></description>
<dc:creator><![CDATA[Proud, C. G.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp012</dc:identifier>
<dc:title><![CDATA[Dynamic Balancing: DEPTOR Tips the Scales]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>63</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>61</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/64?rss=1">
<title><![CDATA[When Shigella Tells the Cell to Hang On]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/64?rss=1</link>
<description><![CDATA[
<p>OspE, a <I>Shigella</I> type III effector binds to integrin-like kinase and enhances cell adhesion to better disseminate and colonize the intestinal epithelium. Because of the existence of OspE orthologues in other enteropathogens such as enteropathogenic <I>Escherichia coli</I> or <I>Salmonella</I> sp., maintenance of cell adhesion appears as a widespread strategy for bacteria that interact with the intestinal epithelium.</p>
]]></description>
<dc:creator><![CDATA[Tran Van Nhieu, G., Guignot, J.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp013</dc:identifier>
<dc:title><![CDATA[When Shigella Tells the Cell to Hang On]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>65</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>64</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/66?rss=1">
<title><![CDATA[BATF: Bringing (in) Another Th17-regulating Factor]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/66?rss=1</link>
<description><![CDATA[
<p>T helper (Th) 17 cells are a recently identified subset of T cells that regulate tissue inflammation, and RORt and ROR have been shown to be Th17-specific transcription factors that mediate Th17 cell generation. A new study of Batf-deficient mice shows that this AP-1 family transcription factor also regulates Th17 cell differentiation by binding to Th17-associated gene promoters and by maintaining ROR and RORt expression, shedding new lights on current clinical modulation of Th17 cell function in inflammatory diseases.</p>
]]></description>
<dc:creator><![CDATA[Martinez, G. J., Dong, C.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp016</dc:identifier>
<dc:title><![CDATA[BATF: Bringing (in) Another Th17-regulating Factor]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>68</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>66</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/69?rss=1">
<title><![CDATA[The Emergence of Basophils as Antigen-Presenting Cells in Th2 Inflammatory Responses]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/69?rss=1</link>
<description><![CDATA[
<p>Basophils gain prominence in Th2 inflammatory responses with the discovery that they function as antigen-presenting cells and are sufficient to drive Th2 cell differentiation.</p>
]]></description>
<dc:creator><![CDATA[Mikhak, Z., Luster, A. D.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp017</dc:identifier>
<dc:title><![CDATA[The Emergence of Basophils as Antigen-Presenting Cells in Th2 Inflammatory Responses]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>71</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>69</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/72?rss=1">
<title><![CDATA[A Pom1 Gradient Is Made to Measure]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/72?rss=1</link>
<description><![CDATA[
<p>In order for cell division to proceed, fission yeast must first attain critical cell size. The mechanism by which size is detected had not been identified until two recent studies showed that cells utilize an intracellular gradient of Pom1p kinase to measure cell length.</p>
]]></description>
<dc:creator><![CDATA[Calvert, M. E.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp020</dc:identifier>
<dc:title><![CDATA[A Pom1 Gradient Is Made to Measure]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>74</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>72</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/75?rss=1">
<title><![CDATA[Cholesterol Worships a New Idol]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/75?rss=1</link>
<description><![CDATA[
<p>The growing worldwide epidemic of cardiovascular disease suggests that new therapeutic strategies are needed to complement statins in the lowering of cholesterol levels. In a recent paper in <I>Science</I>, Tontonoz and colleagues have identified Idol as a protein that can control cholesterol levels by regulating the stability of the low-density lipoprotein receptor; inhibiting the activity of Idol could provide novel approaches for the treatment of cardiovascular disease.</p>
]]></description>
<dc:creator><![CDATA[Schulman, I. G.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp022</dc:identifier>
<dc:title><![CDATA[Cholesterol Worships a New Idol]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>76</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>75</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/77?rss=1">
<title><![CDATA[Innate Immune Cells Cast an Eye on DNA]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/77?rss=1</link>
<description><![CDATA[
<p>The threonine phosphatase eyes absent (EYA) has been identified as a novel regulator of innate immune responses to cytosolic nucleic acids and undigested DNA from apoptotic cells. EYA regulates responses of yet unidentified DNA sensors and enhances interferon-&beta; and CXCL10 transcription.</p>
]]></description>
<dc:creator><![CDATA[Sander, L. E., Blander, J. M.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp023</dc:identifier>
<dc:title><![CDATA[Innate Immune Cells Cast an Eye on DNA]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>79</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>77</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/80?rss=1">
<title><![CDATA[Another Facet of Ubiquitylation: Death]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/80?rss=1</link>
<description><![CDATA[
<p>Ubiquitylation of caspase-8 by the Cullin3 E3 ligase allows its translocation to cytosolic aggregates in the cell by p62/sequestosome-1, increasing caspase-8 activation and thus leading to TRAIL-induced cell death.</p>
]]></description>
<dc:creator><![CDATA[Wong, W. W.-L., Silke, J.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp019</dc:identifier>
<dc:title><![CDATA[Another Facet of Ubiquitylation: Death]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>81</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>80</prism:startingPage>
<prism:section>Research Highlights</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/82?rss=1">
<title><![CDATA[The TET Family of Proteins: Functions and Roles in Disease]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/82?rss=1</link>
<description><![CDATA[
<p>Translocated in liposarcoma, Ewing's sarcoma and TATA-binding protein-associated factor 15 constitute an interesting and important family of proteins known as the TET proteins. The proteins function in several aspects of cell growth control, including multiple different steps in gene expression, and they are also found mutated in a number of specific diseases. For example, all contain domains for binding nucleic acids and have been shown to function in both RNA polymerase II-mediated transcription and pre-mRNA splicing, possibly connecting these two processes. Chromosomal translocations in human sarcomas result in a fusion of the amino terminus of these proteins, which contains a transcription activation domain, to the DNA-binding domain of a transcription factor. Although the fusion proteins have been characterized in a clinical environment, the function of the cognate full-length protein in normal cells is a more recent topic of study. The first part of this review will describe the TET proteins, followed by detailed descriptions of their multiple roles in cells. The final sections will examine changes that occur in gene regulation in cells expressing the fusion proteins. The clinical implications and treatment of sarcomas will not be addressed but have recently been reviewed.</p>
]]></description>
<dc:creator><![CDATA[Tan, A. Y., Manley, J. L.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp025</dc:identifier>
<dc:title><![CDATA[The TET Family of Proteins: Functions and Roles in Disease]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>92</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>82</prism:startingPage>
<prism:section>Review</prism:section>
</item>

<item rdf:about="http://jmcb.oxfordjournals.org/cgi/content/short/1/2/93?rss=1">
<title><![CDATA[Dazl Promotes Germ Cell Differentiation from Embryonic Stem Cells]]></title>
<link>http://jmcb.oxfordjournals.org/cgi/content/short/1/2/93?rss=1</link>
<description><![CDATA[
<p>It has been demonstrated that through the formation of embryoid bodies (EBs) germ cells can be derived from embryonic stem (ES) cells. Here, we describe a transgene expression approach to derive germ cells directly from ES cells <I>in vitro</I> without EB formation. Through the ectopic expression of Deleted in Azoospermia-Like (Dazl), a germ cell-specific RNA-binding protein, both motile tailed-sperm and oocytes were induced from mouse ES (mES) cells in culture. Furthermore, transient overexpression of Dazl led to suppression of Nanog but induced germ cell nuclear antigen in mES cells. Dazl knockdown resulted in reduction in the expression of germ cell markers including Stella, MVH and Prdm1. Our study indicates that Dazl is a master gene controlling germ cell differentiation and that ectopic expression of Dazl promotes the dynamic differentiation of mouse ES cells into gametes <I>in vitro</I>.</p>
]]></description>
<dc:creator><![CDATA[Yu, Z., Ji, P., Cao, J., Zhu, S., Li, Y., Zheng, L., Chen, X., Feng, L.]]></dc:creator>
<dc:date>Fri, 20 Nov 2009 07:56:31 PST</dc:date>
<dc:identifier>info:doi/10.1093/jmcb/mjp026</dc:identifier>
<dc:title><![CDATA[Dazl Promotes Germ Cell Differentiation from Embryonic Stem Cells]]></dc:title>
<dc:publisher>Chinese Academy of Sciences</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>103</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>93</prism:startingPage>
<prism:section>Original Article</prism:section>
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