Li-En Jao, Ph.D.
4415 Tupper Hall
For more information, please visit the Jao Lab Website.
The roles of centrosomes and cilia in development and disease
My laboratory is interested in understanding how the centrosome and its related organelles such as the cilium coordinate signals that regulate cell function and influence development.
The centrosome consists of a pair of centrioles and the surrounding pericentriolar material (PCM), and serves as the main microtubule-organizing center in animal cells. The composition of the PCM is dynamically regulated throughout the cell cycle. Recent studies show that the PCM adopts an orderly organization, instead of an amorphous “cloud” suggested by earlier studies. However, the functional significance of this structured but yet dynamic PCM arrangement is largely unknown. The centrosome also plays essential roles in establishment of cell polarity and regulation of asymmetric cell division. In differentiated cells, the “mother” centriole (the older of the pair) can transform into the basal body, from which two types of microtubule structures—motile and primary (non-motile) cilia—nucleate and protrude from the cell surface. Motile cilia are restricted to certain populations of cells, including those in the airway, brain ventricle, and oviducts, and exhibit a rhythmic beating motion. They function, for example, to clear the mucus in the airway. However, the non-motile primary cilia are present in nearly all cells and are thought to act as a sensory “antenna” for the cell.
Dysfunction of centrosomes and cilia has been linked to a plethora of human diseases, including cancer, dwarfism, microcephaly (disorders with small head size), and various ciliopathies (diseases caused by dysfunction of cilia). However, little is known about how the perturbation of these centrosome-related functions leads to a wide spectrum of disorders.
Using a combination of approaches encompassing proteomics, cell biology, zebrafish genetics, and in vivo live microscopy, we aim to dissect the roles of centrosomes and cilia in various biological contexts, including neurogenesis and cell signaling. Our research goal is to bridge the knowledge gap between centrosomal dysfunction and manifestation of disease phenotypes. Understanding the gene-phenotype relationship is the first step to therapeutic intervention for centrosome-related disorders.
Some of the questions we are pursuing include:
- How is centrosomal dysfunction translated into developmental defects such as microcephaly during early vertebrate neurogenesis?
- How is PCM remodeling regulated at different cell cycle stages?
- What is the role of the PCM in centriole maturation and ciliogenesis?
- How is the coordinated movement of motile cilia achieved?
Sepulveda G, Antkowiak M, Brust-Mascher I, Mahe K, Ou T, Castro N, Christensen LN, Cheung L, Jiang X, Yoon D, Huang B, and Jao LE (2018). Co-translational protein targeting facilitates centrosomal recruitment of PCNT during centrosome maturation in vertebrates. eLife 2018;7:e34959 DOI: 10.7554/eLife.34959
Susman MW, Karuna EP, Kunz RC, Gujral TS, Cantú AV, Choi SS, Jong BY, Okada K, Scales MK, Hum J, Hu LS, Kirschner MW, Nishinakamura R, Yamada S, Laird DJ, Jao LE, Gygi SP, Greenberg ME, and Ho HH (2017). Kinesin superfamily protein Kif26b links Wnt5a-Ror signaling to the control of cell and tissue behaviors in vertebrates. eLife. 2017 Sep 8;6. pii: e26509. doi: 10.7554/eLife.26509.
Jao LE*, Akef A, and Wente SR (2017). A role for Gle1, a regulator of DEAD-box RNA helicases, at centrosomes and basal bodies. Molecular Biology of the Cell 28: 120-127.
Liu LY, Lin MH, Lai ZY, Jiang JP, Huang YC, Jao LE, and Chuang YJ (2016). Motor neuron-derived Thsd7a is essential for zebrafish vascular development via the Notch-dll4 signaling pathway. Journal of Biomedical Science 23: 59-69.
Kaneb HM, Folkmann AW, Belzil VV, Jao LE, Leblond CS, Girard SL, Daoud H, Noreau A, Rochefort D, Hince P, Szuto A, Vidal S, André-Guimont C, Camu W, Bouchard JP, Dupré J, Meininger V, Rouleau GA, Wente SR, and Dion PA (2015). Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics 24: 1363-1373.
Jao LE, Wente SR, Chen W (2013). Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system. Proc. Natl. Acad. Sci. USA. 110:13904-13909.
Varshney GK, Lu J, Gildea DE, Huang H, Pei W, Yang Z, Huang SC, Schoenfeld D, Pho N, Diaz-Cano DC, Hirase T, Moshbrook-Davis D, Zhang S, Jao LE, Zhang B, Wolfsberg TG, Pellegrini M, Burgess SM, and Lin S (2013). A large-scale zebrafish gene knockout resource for the genome-wide study of gene function. Genome Research 23: 727-735.
Jao LE, Appel B, and Wente SR (2012). A zebrafish model of lethal congenital contracture syndrome 1 reveals Gle1 function in spinal neural precursor survival and motor axon arborization. Development 139: 1316-1326.
Wang D*, Jao LE*, Zheng N, Dolan K, Ivey J, Zonies S, Wu X, Wu K, Yang H, Meng Q, Zhu Z, Zhang B, Lin S, and Burgess SM (2007). Efficient genome-wide mutagenesis of zebrafish genes by retroviral insertions. Proc. Natl. Acad. Sci. USA. 104: 12428-12433.
Jao DL and Chen KY (2006) Tandem affinity purification revealed the hypusine-dependent binding of eukaryotic initiation factor 5A to the translating 80S ribosomal complex. J. Cell. Biochem. 97: 583-598.