TY - JOUR
T1 - Systematic analysis of neural projections reveals clonal composition of the Drosophila brain
AU - Ito, Masayoshi
AU - Masuda, Naoki
AU - Shinomiya, Kazunori
AU - Endo, Keita
AU - Ito, Kei
N1 - Funding Information:
We are grateful to N. Strausfeld and K. Hanashima for discussion. We thank T. Awasaki and T. Lee for communicating results prior to publication; B. Dickson, M. Ramaswami, and the Bloomington Drosophila Stock Center for fly strains; J. Tanimura for sharing antibody-labeling data; and S. Shuto, K. Yamashita, and H. Hirose for technical assistance. This work was supported by a CREST/JST grant to K.I. and Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan to K.I. and N.M. The transgenic animal experiments are approved by the review board of IMCB.
PY - 2013/4/22
Y1 - 2013/4/22
N2 - Background: During development neurons are generated by sequential divisions of neural stem cells, or neuroblasts. In the insect brain progeny of certain stem cells form lineage-specific sets of projections that arborize in distinct brain regions, called clonal units. Though this raises the possibility that the entire neural network in the brain might be organized in a clone-dependent fashion, only a small portion of clones has been identified. Results: Using Drosophila melanogaster, we randomly labeled one of about 100 stem cells at the beginning of the larval stage, analyzed the projection patterns of their progeny in the adult, and identified 96 clonal units in the central part of the fly brain, the cerebrum. Neurons of all the clones arborize in distinct regions of the brain, though many clones feature heterogeneous groups of neurons in terms of their projection patterns and neurotransmitters. Arborizations of clones overlap preferentially to form several groups of closely associated clones. Fascicles and commissures were all made by unique sets of clones. Whereas well-investigated brain regions such as the mushroom body and central complex consist of relatively small numbers of clones and are specifically connected with a limited number of neuropils, seemingly disorganized neuropils surrounding them are composed by a much larger number of clones and have extensive specific connections with many other neuropils. Conclusions: Our study showed that the insect brain is formed by a composition of cell-lineage-dependent modules. Clonal analysis reveals organized architecture even in those neuropils without obvious structural landmarks.
AB - Background: During development neurons are generated by sequential divisions of neural stem cells, or neuroblasts. In the insect brain progeny of certain stem cells form lineage-specific sets of projections that arborize in distinct brain regions, called clonal units. Though this raises the possibility that the entire neural network in the brain might be organized in a clone-dependent fashion, only a small portion of clones has been identified. Results: Using Drosophila melanogaster, we randomly labeled one of about 100 stem cells at the beginning of the larval stage, analyzed the projection patterns of their progeny in the adult, and identified 96 clonal units in the central part of the fly brain, the cerebrum. Neurons of all the clones arborize in distinct regions of the brain, though many clones feature heterogeneous groups of neurons in terms of their projection patterns and neurotransmitters. Arborizations of clones overlap preferentially to form several groups of closely associated clones. Fascicles and commissures were all made by unique sets of clones. Whereas well-investigated brain regions such as the mushroom body and central complex consist of relatively small numbers of clones and are specifically connected with a limited number of neuropils, seemingly disorganized neuropils surrounding them are composed by a much larger number of clones and have extensive specific connections with many other neuropils. Conclusions: Our study showed that the insect brain is formed by a composition of cell-lineage-dependent modules. Clonal analysis reveals organized architecture even in those neuropils without obvious structural landmarks.
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U2 - 10.1016/j.cub.2013.03.015
DO - 10.1016/j.cub.2013.03.015
M3 - Article
C2 - 23541729
AN - SCOPUS:84876751827
SN - 0960-9822
VL - 23
SP - 644
EP - 655
JO - Current Biology
JF - Current Biology
IS - 8
ER -