TY - JOUR
T1 - MBR-1, a novel helix-turn-helix transcription factor, is required for pruning excessive neurites in Caenorhabditis elegans
AU - Kage, Eriko
AU - Hayashi, Yu
AU - Takeuchi, Hideaki
AU - Hirotsu, Takaaki
AU - Kunitomo, Hirofumi
AU - Inoue, Takao
AU - Arai, Hiroyuki
AU - Iino, Yuichi
AU - Kubo, Takeo
N1 - Funding Information:
We are grateful to Drs. Oliver Hobert (Columbia University) for providing OtIs14 , Andrew Fire for pPD49.26, pPD95.75, and pPD119.45, and Adam Wenick and Oliver Hobert (Columbia University) for sharing of the unpublished strain him-8(e1489) IV;Is[unc-122::gfp, P ttx-3 ::rfp] ; to the Sanger Center for the Cosmid T01C1; and to the C. elegans Sequence Consortium for sequence information. Several strains were kindly provided by the Caenorhabditis Genetics Center, which is supported by the National Institutes of Health National Center for Research Resources. We are also grateful to Drs. Asako Sugimoto (RIKEN Center for Developmental Biology) and Masayuki Yamamoto (University of Tokyo) for their kind technical assistance in handling nematodes at the early stage of our research. The TMP/UV-mutagenized C. elegans library was generated by Ms. Yuka Suzuki in the laboratory of H.A. The P mbr-1 ::gfp vector and strain were made by Yoshihisa Mita in the laboratory of T.K. This work was supported by Grants-in-Aid from the Bio-oriented Technology Research Advancement Institution of Japan and Japan Foundation for Applied Entomology. Y.H. is the recipient of a fellowship from the Japan Society for the Promotion of Science for Young Scientists.
PY - 2005/9/6
Y1 - 2005/9/6
N2 - In the developing brain, excessive neurites are actively pruned in the construction and remodeling of neural circuits. We demonstrate for the first time that the pruning of neurites occurs in the simple neural circuit of Caenorhabditis elegans and that a novel transcription factor, MBR-1, is involved in this process. We identified MBR-1 as a C. elegans ortholog of Mblk-1, a transcription factor that is expressed preferentially in the mushroom bodies of the honeybee brain [1]. Although Mblk-1 homologs are conserved among animal species, their roles in the nervous system have never been analyzed. We used C. elegans as an ideal model animal for analysis of neuronal development. mbr-1 is expressed in various neurons in the head and tail ganglia. A comparison of the morphology of mbr-1-expressing neurons revealed that excessive neurites connecting the left and right AIM interneurons are eliminated during larval stages in wild-type but are sustained through the adult stage in the mbr-1 mutant. In addition, mbr-1 expression is regulated by UNC-86, a POU domain transcription factor, and the pruning of the excessive AIM connection is impaired in the unc-86 mutant. These findings provide an important clue for further genetic dissection of neurite pruning.
AB - In the developing brain, excessive neurites are actively pruned in the construction and remodeling of neural circuits. We demonstrate for the first time that the pruning of neurites occurs in the simple neural circuit of Caenorhabditis elegans and that a novel transcription factor, MBR-1, is involved in this process. We identified MBR-1 as a C. elegans ortholog of Mblk-1, a transcription factor that is expressed preferentially in the mushroom bodies of the honeybee brain [1]. Although Mblk-1 homologs are conserved among animal species, their roles in the nervous system have never been analyzed. We used C. elegans as an ideal model animal for analysis of neuronal development. mbr-1 is expressed in various neurons in the head and tail ganglia. A comparison of the morphology of mbr-1-expressing neurons revealed that excessive neurites connecting the left and right AIM interneurons are eliminated during larval stages in wild-type but are sustained through the adult stage in the mbr-1 mutant. In addition, mbr-1 expression is regulated by UNC-86, a POU domain transcription factor, and the pruning of the excessive AIM connection is impaired in the unc-86 mutant. These findings provide an important clue for further genetic dissection of neurite pruning.
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U2 - 10.1016/j.cub.2005.07.057
DO - 10.1016/j.cub.2005.07.057
M3 - Article
C2 - 16139210
AN - SCOPUS:24044506250
SN - 0960-9822
VL - 15
SP - 1554
EP - 1559
JO - Current Biology
JF - Current Biology
IS - 17
ER -