Lineage-specific effects of Notch/Numb signaling in post-embryonic development of the Drosophila brain
Author(s) -
Suewei Lin,
Sen-Lin Lai,
HungHsiang Yu,
Takahiro Chihara,
Liqun Luo,
Tzumin Lee
Publication year - 2009
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.041699
Subject(s) - numb , biology , neuroblast , notch signaling pathway , lineage (genetic) , cell fate determination , embryonic stem cell , neurogenesis , neural stem cell , microbiology and biotechnology , progenitor cell , proneural genes , genetics , neuroscience , stem cell , signal transduction , transcription factor , gene
Numb can antagonize Notch signaling to diversify the fates of sister cells. We report here that paired sister cells acquire different fates in all three Drosophila neuronal lineages that make diverse types of antennal lobe projection neurons (PNs). Only one in each pair of postmitotic neurons survives into the adult stage in both anterodorsal (ad) and ventral (v) PN lineages. Notably, Notch signaling specifies the PN fate in the vPN lineage but promotes programmed cell death in the missing siblings in the adPN lineage. In addition, Notch/Numb-mediated binary sibling fates underlie the production of PNs and local interneurons from common precursors in the lAL lineage. Furthermore, Numb is needed in the lateral but not adPN or vPN lineages to prevent the appearance of ectopic neuroblasts and to ensure proper self-renewal of neural progenitors. These lineage-specific outputs of Notch/Numb signaling show that a universal mechanism of binary fate decision can be utilized to govern diverse neural sibling differentiations.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom