MLL1 is essential for retinal neurogenesis and horizontal inner neuron integrity

被引:12
|
作者
Brightman, Diana S. [1 ,3 ,6 ]
Grant, Rachel L. [5 ]
Ruzycki, Philip A. [4 ]
Suzuki, Ray [5 ]
Hennig, Anne K. [1 ]
Chen, Shiming [1 ,2 ]
机构
[1] Washington Univ, Dept Ophthalmol & Visual Sci, St Louis, MO 63130 USA
[2] Washington Univ, Dept Dev Biol, St Louis, MO 63130 USA
[3] Washington Univ, Div Biol & Biomed Sci, Mol Cell Biol Grad Program, St Louis, MO USA
[4] Washington Univ, Div Biol & Biomed Sci, Mol Genet & Genom Grad Program, St Louis, MO USA
[5] Washington Univ, Coll Arts & Sci, St Louis, MO USA
[6] Cincinnati Childrens Hosp Med Ctr, 3333 Burnet Ave, Cincinnati, OH 45229 USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
CELL FATE DETERMINATION; HISTONE-METHYLTRANSFERASE; PROGENITOR PROLIFERATION; DROSOPHILA-TRITHORAX; SYNAPTIC PLASTICITY; HOMEOBOX GENE; CHX10; INACTIVATION; MAINTENANCE; EXPRESSION;
D O I
10.1038/s41598-018-30355-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Development of retinal structure and function is controlled by cell type-specific transcription factors and widely expressed co-regulators. The latter includes the mixed-lineage leukemia (MLL) family of histone methyltransferases that catalyze histone H3 lysine 4 di- and tri-methylation associated with gene activation. One such member, MLL1, is widely expressed in the central nervous system including the retina. However, its role in retinal development is unknown. To address this question, we knocked out Mll1 in mouse retinal progenitors, and discovered that MLL1 plays multiple roles in retinal development by regulating progenitor cell proliferation, cell type composition and neuron-glia balance, maintenance of horizontal neurons, and formation of functional synapses between neuronal layers required for visual signal transmission and processing. Altogether, our results suggest that MLL1 is indispensable for retinal neurogenesis and function development, providing a new paradigm for cell type-specific roles of known histone modifying enzymes during CNS tissue development.
引用
收藏
页数:17
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