Functional Repression of Islet-2 by Disruption of Complex with Ldb Impairs Peripheral Axonal Outgrowth in Embryonic Zebrafish

نویسندگان

  • Hiroshi Segawa
  • Toshio Miyashita
  • Yoshikazu Hirate
  • Shin-ichi Higashijima
  • Naoichi Chino
  • Keiichi Uyemura
  • Yutaka Kikuchi
  • Hitoshi Okamoto
چکیده

Islet-2 is a LIM/homeodomain-type transcription factor of the Islet-1 family expressed in embryonic zebrafish. Two Islet-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.

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عنوان ژورنال:
  • Neuron

دوره 30  شماره 

صفحات  -

تاریخ انتشار 2001