Journal
CELLULAR MICROBIOLOGY
Volume 16, Issue 4, Pages 482-489Publisher
WILEY
DOI: 10.1111/cmi.12268
Keywords
-
Categories
Funding
- Public Health Service from the National Institute of Allergy and Infectious Diseases [AI28798, AI56333, AI043594]
Ask authors/readers for more resources
One of the key questions in understanding the biology of an organism is how to correlate cellular fate and function with gene expression patterns. This is particularly relevant for pathogenic organisms, like the parasitic protozoa Trypanosoma brucei, who often cycle between different hosts, thereby encountering vastly different environments. Survival in and adaptation to new surroundings requires activation of specific gene networks, which is most often achieved by regulatory mechanisms embedded in the transcriptional machinery. However, in T.brucei and related trypanosomatids these responses appear to be accomplished mainly by post-transcriptional mechanisms. Although an understanding of how this parasite modulates gene regulatory networks is in the early stages, RNA-binding proteins (RBPs) are beginning to take centre stage. Here, we discuss recent progress in the identification of RBPs with crucial roles in different stages of the T.brucei life cycle, and in elucidating targets of RBPs.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available