Transcriptional Control of the Development and Function of Vα14i NKT Cells

Author(s):  
Isaac Engel ◽  
Mitchell Kronenberg
2014 ◽  
Vol 5 (5) ◽  
pp. 371-382 ◽  
Author(s):  
Suyan Li ◽  
Sampada Joshee ◽  
Anju Vasudevan

AbstractMidbrain GABA neurons, endowed with multiple morphological, physiological and molecular characteristics as well as projection patterns are key players interacting with diverse regions of the brain and capable of modulating several aspects of behavior. The diversity of these GABA neuronal populations based on their location and function in the dorsal, medial or ventral midbrain has challenged efforts to rapidly uncover their developmental regulation. Here we review recent developments that are beginning to illuminate transcriptional control of GABA neurons in the embryonic midbrain (mesencephalon) and discuss its implications for understanding and treatment of neurological and psychiatric illnesses.


Obesity ◽  
2018 ◽  
Vol 27 (1) ◽  
pp. 13-21 ◽  
Author(s):  
Suzanne N. Shapira ◽  
Patrick Seale

Oncotarget ◽  
2016 ◽  
Vol 7 (43) ◽  
pp. 71001-71012 ◽  
Author(s):  
Yan Li ◽  
Qing Yu ◽  
Zhengguo Zhang ◽  
Jian Wang ◽  
Simin Li ◽  
...  

2004 ◽  
Vol 172 (10) ◽  
pp. 6115-6122 ◽  
Author(s):  
Motoi Maeda ◽  
Ashleen Shadeo ◽  
Anna M. MacFadyen ◽  
Fumio Takei

2001 ◽  
Vol 183 (1) ◽  
pp. 46-54 ◽  
Author(s):  
Yvonne Weber ◽  
Uwe J. Santore ◽  
Joachim F. Ernst ◽  
Rolf K. Swoboda

ABSTRACT Sec20p is a component of the yeast Saccharomyces cerevisiae secretory pathway that does not have a close homolog in higher eukaryotic cells. To verify the function of Sec20p in other fungal species, we characterized the gene encoding a Sec20p homolog in the human fungal pathogen Candida albicans. The deduced protein has 27% identity with, but is missing about 100 N-terminal residues compared to S. cerevisiae Sec20p, which is part of the cytoplasmic tail interacting with the cytoplasmic protein Tip20p. Because a strain lacking both C. albicans SEC20alleles could not be constructed, we placed SEC20 under transcriptional control of two regulatable promoters, MET3pand PCK1p. Repression of SEC20 expression in these strains prevented (MET3p-SEC20 allele) or retarded (PCK1p-SEC20 allele) growth and led to the appearance of extensive intracellular membranes, which frequently formed stacks. Reduced SEC20 expression in the PCK1p-SEC20strain did not affect morphogenesis but led to a series of hypersensitivity phenotypes including supersensitivity to aminoglycoside antibiotics, to nystatin, to sodium dodecyl sulfate, and to cell wall inhibitors. These results demonstrate the occurrence and function of Sec20p in a fungal species other than S. cerevisiae, but the lack of the N-terminal domain and the apparent absence of a close TIP20 homolog in the C. albicans genome also indicate a considerable diversity in mechanisms of retrograde vesicle traffic in eukaryotes.


2015 ◽  
Vol 35 (suppl_1) ◽  
Author(s):  
Ruben G de Bruin ◽  
Lily Shiue ◽  
Anjana Djarmshi ◽  
Hetty C de Boer ◽  
Wai Yi Leung ◽  
...  

A hallmark of inflammatory diseases is the excessive recruitment and influx of monocytes to sites of tissue damage and their ensuing differentiation into macrophages. Numerous stimuli are known to induce new transcription necessary for macrophage identity, but post-transcriptional control of human macrophage differentiation is less well understood. Here, we detail our discovery that levels of the RNA-binding protein Quaking (QKI) are low in monocytes of early atherosclerotic lesions, but abundant in macrophages of advanced plaques. Specific depletion of QKI protein impaired monocyte adhesion, migration and differentiation into macrophages, and lesion formation. RNA-seq and microarray analysis of human monocyte and macrophage transcriptomes, including those of a unique QKI haploinsufficient patient, reveal developmental changes in RNA levels and alternative splicing of RNA transcripts enriched in QKI-bound sequence elements. The importance of these transcripts and requirement for QKI during differentiation illustrates a central role for QKI in post-transcriptionally guiding macrophage identity and function. These studies implicate QKI as a novel target for therapeutic intervention in inflammatory diseases.


2009 ◽  
Vol 70 (4) ◽  
pp. 262-268 ◽  
Author(s):  
Alejandro Roman-Gonzalez ◽  
Maria Eugenia Moreno ◽  
Juan Manuel Alfaro ◽  
Federico Uribe ◽  
Guillermo Latorre-Sierra ◽  
...  

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