Ikaros Confers Early Temporal Competence to Mouse Retinal Progenitor Cells

被引:160
作者
Elliott, Jimmy [1 ]
Jolicoeur, Christine [1 ]
Ramamurthy, Vasanth [1 ]
Cayouette, Michel [1 ,2 ,3 ,4 ]
机构
[1] Inst Rech Clin Montreal, Cellular Neurobiol Res Unit, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Dept Med, Montreal, PQ H3T 1J4, Canada
[3] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 2B2, Canada
[4] McGill Univ, Div Expt Med, Montreal, PQ H3A 2B2, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.neuron.2008.08.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the developing mouse retina, multipotent retinal progenitor cells (RPCs) give rise to specific retinal cell types at different times, but the molecular mechanisms regulating how RPCs change over time remain unclear. In the Drosophila neuroblast lineage, the zinc finger transcription factor Hunchback (Hb) is both necessary and sufficient to specify early-born neuronal identity. We show here that Ikaros, a mouse ortholog of Hb, is expressed in all early embryonic RPCs, which then give rise to Ikaros-negative RPCs at later stages in the lineage. Remarkably, misexpression of Ikaros in late RPCs is sufficient to confer competence to generate early-born neurons. Conversely, Ikaros mutant mice have reduced numbers of early-born cell types, whereas late-born cell types are not affected. These results suggest a model in which Ikaros expression is both necessary and sufficient to confer early temporal competence to RPCs and raise the possibility that a similar strategy might be used to control the sequential order of cell birth in other parts of the nervous system.
引用
收藏
页码:26 / 39
页数:14
相关论文
共 53 条
[1]   Ikaros is expressed in developing striatal neurons and involved in enkephalinergic differentiation [J].
Agoston, Denes V. ;
Szemes, Marianna ;
Dobi, Albert ;
Palkovits, Miklos ;
Georgopoulos, Katia ;
Gyorgy, Andrea ;
Ring, Mary A. .
JOURNAL OF NEUROCHEMISTRY, 2007, 102 (06) :1805-1816
[2]   Programmed transformations in neuroblast gene expression during Drosophila CNS lineage development [J].
Brody, T ;
Odenwald, WF .
DEVELOPMENTAL BIOLOGY, 2000, 226 (01) :34-44
[3]  
Brown NL, 1998, DEVELOPMENT, V125, P4821
[4]   Importance of intrinsic mechanisms in cell fate decisions in the developing rat retina [J].
Cayouette, M ;
Barres, BA ;
Raff, M .
NEURON, 2003, 40 (05) :897-904
[5]   Asymmetric segregation of numb in retinal development and the influence of the pigmented epithelium [J].
Cayouette, M ;
Whitmore, AV ;
Jeffery, G ;
Raff, M .
JOURNAL OF NEUROSCIENCE, 2001, 21 (15) :5643-5651
[6]   Lineage in the vertebrate retina [J].
Cayouette, Michel ;
Poggi, Lucia ;
Harris, William A. .
TRENDS IN NEUROSCIENCES, 2006, 29 (10) :563-570
[7]   Cell fate determination in the vertebrate retina [J].
Cepko, CL ;
Austin, CP ;
Yang, XJ ;
Alexiades, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :589-595
[8]  
Christopherson I, 2001, J LEUKOCYTE BIOL, V69, P675
[9]   Targeting of Ikaros to pericentromeric heterochromatin by direct DNA binding [J].
Cobb, BS ;
Morales-Alcelay, S ;
Kleiger, G ;
Brown, KE ;
Fisher, AG ;
Smale, ST .
GENES & DEVELOPMENT, 2000, 14 (17) :2146-2160
[10]  
Cobb BS, 2005, CURR TOP MICROBIOL, V290, P29