A Distinct Set of Drosophila Brain Neurons Required for Neurofibromatosis Type 1-Dependent Learning and Memory

被引:45
作者
Buchanan, Monica E. [1 ]
Davis, Ronald L. [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
MUSHROOM BODY NEURONS; PREFERENTIAL EXPRESSION; ADENYLATE-CYCLASE; MUTANT DROSOPHILA; OLFACTORY MEMORY; TERM-MEMORY; TRACE; GENE; RESCUE; IMPAIRMENT;
D O I
10.1523/JNEUROSCI.0283-10.2010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nonspecific cognitive impairments are one of the many manifestations of neurofibromatosis type 1 (NF1). A learning phenotype is also present in Drosophila melanogaster that lack a functional neurofibromin gene (nf1). Multiple studies have indicated that Nf1-dependent learning in Drosophila involves the cAMP pathway, including the demonstration of a genetic interaction between Nf1 and the rutabaga-encoded adenylyl cyclase (Rut-AC). Olfactory classical conditioning experiments have previously demonstrated a requirement for Rut-AC activity and downstream cAMP pathway signaling in neurons of the mushroom bodies. However, Nf1 expression in adult mushroom body neurons has not been observed. Here, we address this discrepancy by demonstrating (1) that Rut-AC is required for the acquisition and stability of olfactory memories, whereas Nf1 is only required for acquisition, (2) that expression of nf1 RNA can be detected in the cell bodies of mushroom body neurons, and (3) that expression of an nf1 transgene only in the alpha/beta subset of mushroom body neurons is sufficient to restore both protein synthesis-independent and protein synthesis-dependent memory. Our observations indicate that memory-related functions of Rut-AC are both Nf1-dependent and -independent, that Nf1 mediates the formation of two distinct memory components within a single neuron population, and that our understanding of Nf1 function in memory processes may be dissected from its role in other brain functions by specifically studying the alpha/beta mushroom body neurons.
引用
收藏
页码:10135 / 10143
页数:9
相关论文
共 37 条
[11]   A neurofibromatosis-1-regulated pathway is required for learning in Drosophila [J].
Guo, HF ;
Tong, JY ;
Hannan, F ;
Luo, L ;
Zhong, Y .
NATURE, 2000, 403 (6772) :895-898
[12]   PREFERENTIAL EXPRESSION OF THE DROSOPHILA RUTABAGA GENE IN MUSHROOM BODIES, NEURAL CENTERS FOR LEARNING IN INSECTS [J].
HAN, PL ;
LEVIN, LR ;
REED, RR ;
DAVIS, RL .
NEURON, 1992, 9 (04) :619-627
[13]   Effect of neurofibromatosis type I mutations on a novel pathway for adenylyl cyclase activation requiring neurofibromin and Ras [J].
Hannan, F ;
Ho, I ;
Tong, JJY ;
Zhu, YH ;
Nurnberg, P ;
Zhong, Y .
HUMAN MOLECULAR GENETICS, 2006, 15 (07) :1087-1098
[14]   Distinct functional domains of neurofibromatosis type 1 regulate immediate versus long-term memory formation [J].
Ho, Ivan Shun ;
Hannan, Frances ;
Guo, Hui-Fu ;
Hakker, Inessa ;
Zhong, Yi .
JOURNAL OF NEUROSCIENCE, 2007, 27 (25) :6852-6857
[15]   TUMOR PREDISPOSITION IN MICE HETEROZYGOUS FOR A TARGETED MUTATION IN NF1 [J].
JACKS, T ;
SHIH, TS ;
SCHMITT, EM ;
BRONSON, RT ;
BERNARDS, A ;
WEINBERG, RA .
NATURE GENETICS, 1994, 7 (03) :353-361
[16]   Sequential use of mushroom body neuron subsets during Drosophila odor memory processing [J].
Krashes, Michael J. ;
Keene, Alex C. ;
Leung, Benjamin ;
Armstrong, J. Douglas ;
Waddell, Scott .
NEURON, 2007, 53 (01) :103-115
[17]   Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis [J].
Lee, T ;
Luo, LQ .
NEURON, 1999, 22 (03) :451-461
[18]   GABAA receptor RDL inhibits Drosophila olfactory associative learning [J].
Liu, Xu ;
Krause, William C. ;
Davis, Ronald L. .
NEURON, 2007, 56 (06) :1090-1102
[19]   Pharmacogenetic rescue in time and space of the rutabaga memory impairment by using Gene-Switch [J].
Mao, ZM ;
Roman, G ;
Zong, L ;
Davis, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (01) :198-203
[20]   Spatiotemporal rescue of memory dysfunction in Drosophila [J].
McGuire, SE ;
Le, PT ;
Osborn, AJ ;
Matsumoto, K ;
Davis, RL .
SCIENCE, 2003, 302 (5651) :1765-1768