Literature DB >> 10454371

Tripartite mushroom body architecture revealed by antigenic markers.

J R Crittenden1, E M Skoulakis, K A Han, D Kalderon, R L Davis.   

Abstract

We have explored the organization of the axonal lobes in Drosophila mushroom bodies by using a panel of immunohistochemical markers. These markers consist of antibodies to eight proteins expressed preferentially in the mushroom bodies: DAMB, DCO, DRK, FASII, LEO, OAMB, PKA RII, and RUT. Previous to this work, four axonal lobes, two projecting dorsally (alpha and alpha') and two medially (beta and gamma), had been described in Drosophila mushroom bodies. However, our analysis of immunohistochemically stained frontal and sagittal sections of the brain revealed three medially projecting lobes. The newly distinguished lobe, which we term beta', lies along the dorsal surface of beta, just posterior to gamma. In addition to resolving a fifth lobe, our studies revealed that there are specific lobe sets defined by equivalent marker expression levels. These sets are (1) the alpha and beta lobes, (2) the alpha' and beta' lobes, and (3) the gamma lobe and heel (a lateral projection formed by a hairpin turn of some of the peduncle fibers). All of the markers we have examined are consistent with these three sets. Previous Golgi studies demonstrate that each mushroom body cell projects one axon that branches into a dorsal lobe and a medial lobe, or one unbranched axon that projects medially. Taken together with the lobe sets listed above, we propose that there are three major projection configurations of mushroom body cell axons: (1) one branch in the alpha and one in the beta lobe, (2) one branch in the alpha' and one in the beta' lobe, and (3) one unbranched axon projecting to the heel and the gamma lobe. The fact that these neuron types exhibit differential expression levels of a number of mushroom body genes suggests that they may have corresponding functional differences. These functions may be conserved in the larvae, as several of these genes were expressed in larval and embryonic mushroom bodies as well. The basic mushroom body structure, including the denritic calyx, peduncle, and lobes, was already visible by the late stages of embryogenesis. With new insights into mushroom body organization, and the characterization of markers for developing mushroom bodies, we are beginning to understand how these structures form and function.

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Year:  1998        PMID: 10454371      PMCID: PMC311260     

Source DB:  PubMed          Journal:  Learn Mem        ISSN: 1072-0502            Impact factor:   2.460


  26 in total

1.  Preferential expression of the Drosophila rutabaga gene in mushroom bodies, neural centers for learning in insects.

Authors:  P L Han; L R Levin; R R Reed; R L Davis
Journal:  Neuron       Date:  1992-10       Impact factor: 17.173

2.  Proliferation pattern of postembryonic neuroblasts in the brain of Drosophila melanogaster.

Authors:  K Ito; Y Hotta
Journal:  Dev Biol       Date:  1992-01       Impact factor: 3.582

3.  The cyclic AMP phosphodiesterase encoded by the Drosophila dunce gene is concentrated in the mushroom body neuropil.

Authors:  A Nighorn; M J Healy; R L Davis
Journal:  Neuron       Date:  1991-03       Impact factor: 17.173

4.  DAMB, a novel dopamine receptor expressed specifically in Drosophila mushroom bodies.

Authors:  K A Han; N S Millar; M S Grotewiel; R L Davis
Journal:  Neuron       Date:  1996-06       Impact factor: 17.173

5.  Distinct mechanisms for synchronization and temporal patterning of odor-encoding neural assemblies.

Authors:  K MacLeod; G Laurent
Journal:  Science       Date:  1996-11-08       Impact factor: 47.728

6.  Ablation of Drosophila photoreceptor cells by conditional expression of a toxin gene.

Authors:  S Kunes; H Steller
Journal:  Genes Dev       Date:  1991-06       Impact factor: 11.361

7.  The Drosophila mushroom body is a quadruple structure of clonal units each of which contains a virtually identical set of neurones and glial cells.

Authors:  K Ito; W Awano; K Suzuki; Y Hiromi; D Yamamoto
Journal:  Development       Date:  1997-02       Impact factor: 6.868

8.  Targeted expression of tetanus toxin light chain in Drosophila specifically eliminates synaptic transmission and causes behavioral defects.

Authors:  S T Sweeney; K Broadie; J Keane; H Niemann; C J O'Kane
Journal:  Neuron       Date:  1995-02       Impact factor: 17.173

9.  Inducible cell ablation in Drosophila by cold-sensitive ricin A chain.

Authors:  K G Moffat; J H Gould; H K Smith; C J O'Kane
Journal:  Development       Date:  1992-03       Impact factor: 6.868

10.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes.

Authors:  A H Brand; N Perrimon
Journal:  Development       Date:  1993-06       Impact factor: 6.868

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  138 in total

Review 1.  What do the mushroom bodies do for the insect brain? an introduction.

Authors:  M Heisenberg
Journal:  Learn Mem       Date:  1998 May-Jun       Impact factor: 2.460

2.  Mapping of the anatomical circuit of CaM kinase-dependent courtship conditioning in Drosophila.

Authors:  M A Joiner; L C Griffith
Journal:  Learn Mem       Date:  1999 Mar-Apr       Impact factor: 2.460

3.  The Drosophila homolog of Down's syndrome critical region 1 gene regulates learning: implications for mental retardation.

Authors:  Karen T Chang; Yi-Jun Shi; Kyung-Tai Min
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-10       Impact factor: 11.205

4.  Identification of mushroom body miniature, a zinc-finger protein implicated in brain development of Drosophila.

Authors:  Thomas Raabe; Susanne Clemens-Richter; Thomas Twardzik; Anselm Ebert; Gertrud Gramlich; Martin Heisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-16       Impact factor: 11.205

5.  Drosophila larvae establish appetitive olfactory memories via mushroom body neurons of embryonic origin.

Authors:  Dennis Pauls; Mareike Selcho; Nanae Gendre; Reinhard F Stocker; Andreas S Thum
Journal:  J Neurosci       Date:  2010-08-11       Impact factor: 6.167

6.  Generating sparse and selective third-order responses in the olfactory system of the fly.

Authors:  Sean X Luo; Richard Axel; L F Abbott
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-24       Impact factor: 11.205

7.  Dissecting neural pathways for forgetting in Drosophila olfactory aversive memory.

Authors:  Yichun Shuai; Areekul Hirokawa; Yulian Ai; Min Zhang; Wanhe Li; Yi Zhong
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-16       Impact factor: 11.205

8.  Drosophila retained/dead ringer is necessary for neuronal pathfinding, female receptivity and repression of fruitless independent male courtship behaviors.

Authors:  Lynn M Ditch; Troy Shirangi; Jeffrey L Pitman; Kristin L Latham; Kim D Finley; Philip T Edeen; Barbara J Taylor; Michael McKeown
Journal:  Development       Date:  2004-12-02       Impact factor: 6.868

9.  Conditional rescue of olfactory learning and memory defects in mutants of the 14-3-3zeta gene leonardo.

Authors:  N Philip; S F Acevedo; E M Skoulakis
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

10.  Drosophila mushroom bodies integrate hunger and satiety signals to control innate food-seeking behavior.

Authors:  Chang-Hui Tsao; Chien-Chun Chen; Chen-Han Lin; Hao-Yu Yang; Suewei Lin
Journal:  Elife       Date:  2018-03-16       Impact factor: 8.140

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