Coordinated genomic control of ciliogenesis and cell movement by RFX2

被引:106
作者
Chung, Mei-I [1 ]
Kwon, Taejoon [1 ]
Tu, Fan [1 ]
Brooks, Eric R. [1 ]
Gupta, Rakhi [2 ]
Meyer, Matthew [1 ]
Baker, Julie C. [2 ]
Marcotte, Edward M. [1 ,3 ,4 ]
Wallingford, John B. [1 ,3 ,4 ,5 ]
机构
[1] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
[2] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[3] Univ Texas Austin, Ctr Syst & Synthet Biol, Austin, TX 78712 USA
[4] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[5] Univ Texas Austin, Howard Hughes Med Inst, Austin, TX 78712 USA
来源
ELIFE | 2014年 / 3卷
关键词
PRIMARY CILIARY DYSKINESIA; HUMAN AIRWAY EPITHELIUM; GENE-EXPRESSION DATA; INTRAFLAGELLAR TRANSPORT; BASAL-CELLS; INTERACTION NETWORKS; STEM-CELLS; PROTEIN; XENOPUS; POLARITY;
D O I
10.7554/eLife.01439
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mechanisms linking systems-level programs of gene expression to discrete cell biological processes in vivo remain poorly understood. In this study, we have defined such a program for multi-ciliated epithelial cells (MCCs), a cell type critical for proper development and homeostasis of the airway, brain and reproductive tracts. Starting from genomic analysis of the cilia-associated transcription factor Rfx2, we used bioinformatics and in vivo cell biological approaches to gain insights into the molecular basis of cilia assembly and function. Moreover, we discovered a previously unrecognized role for an Rfx factor in cell movement, finding that Rfx2 cell-autonomously controls apical surface expansion in nascent MCCs. Thus, Rfx2 coordinates multiple, distinct gene expression programs in MCCs, regulating genes that control cell movement, ciliogenesis, and cilia function. As such, the work serves as a paradigm for understanding genomic control of cell biological processes that span from early cell morphogenetic events to terminally differentiated cellular functions.
引用
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页数:22
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