Functional repression of islet-2 by disruption of complex with Ldb impairs peripheral axonal outgrowth in embryonic zebrafish

被引:87
作者
Segawa, H
Miyashita, T
Hirate, Y
Higashijima, S
Chino, N
Uyemura, K
Kikuchi, Y
Okamoto, H
机构
[1] RIKEN, Brain Sci Inst, Lab Dev Gene Regulat, Wako, Saitama 3510198, Japan
[2] Core Res Evolut Sci & Technol, Japan Sci & Technol Corp, Kawaguchi, Saitama, Japan
[3] Precursory Res Embryon Sci & Technol, JST, Inheritance & Variat Grp, Kawaguchi, Saitama 3320012, Japan
[4] Keio Univ, Sch Med, Dept Rehabil Med, Shinjuku Ku, Tokyo 1600016, Japan
[5] Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, Tokyo 1600016, Japan
[6] Nara Inst Sci & Technol, Grad Sch Biol Sci, Nara 6300101, Japan
[7] Saitama Univ, Fac Sci, Dept Regulat Biol, Saitama 3388570, Japan
关键词
D O I
10.1016/S0896-6273(01)00283-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Islet-2 is a LIM/homeodomain-type transcription factor of the Islet-1 family expressed in embryonic zebrafish. Two lslet-2 molecules bind to the LIM domain binding protein (Ldb) dimers. Overexpression of the LIM domains of Islet-2 or the LIM-interacting domain of Ldb proteins prevented binding of Islet-2 to Ldb proteins in vitro and caused similar in vivo defects in positioning, peripheral axonal outgrowth, and neurotransmitter expression by the Islet-2-positive primary sensory and motor neurons as the defects induced by injection of Islet-2-specific antisense morpholino oligonucleotide. These and other experiments, i.e., mosaic analysis, coexpression of full-length Islet-2, and overexpression of the chimeric LIM domains derived from two different Islet-1 family members, demonstrated that Islet-2 regulates neuronal differentiation by forming a complex with Ldb dimers and possibly with some other Islet-2-specific cofactors.
引用
收藏
页码:423 / 436
页数:14
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