Monoallelic yet combinatorial expression of variable exons of the protocadherin-α gene cluster in single neurons

被引:206
作者
Esumi, S
Kakazu, N
Taguchi, Y
Hirayama, T
Sasaki, A
Hirabayashi, T
Koide, T
Kitsukawa, T
Hamada, S
Yagi, T
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Labs Integrated Biol, KOKORO Biol Grp, Suita, Osaka 5650871, Japan
[2] Japan Sci & Technol Agcy, Core Res Evolut Sci & Technol, Kawaguchi, Saitama 3320012, Japan
[3] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Mol Targeting Canc Prevent, Kamigyo Ku, Kyoto 6028566, Japan
[4] Natl Inst Physiol Sci, Dept Informat Physiol, Div Neurobiol & Behav Genet, Okazaki, Aichi 4448585, Japan
[5] Natl Inst Genet, Mouse Genom Resource Lab, Mishima, Shizuoka 4118540, Japan
[6] Natl Inst Basic Biol, Div Brain Biol, Okazaki, Aichi 4440867, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1038/ng1500
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Diverse protocadherin-alpha genes (Pcdha, also called cadherin-related neuronal receptor or CNR) are expressed in the vertebrate brain. Their genomic organization involves multiple variable exons and a set of constant exons, similar to the immunoglobulin (Ig) and T-cell receptor (TCR) genes. This diversity can be used to distinguish neurons. Using polymorphisms that distinguish the C57BL/6 and MSM mouse strains, we analyzed the allelic expression of the Pcdha gene cluster in individual neurons. Single-cell analysis of Purkinje cells using multiple RT-PCR reactions showed the monoallelic and combinatorial expression of each variable exon in the Pcdha genes. This report is the first description to our knowledge of the allelic expression of a diversified receptor family in the central nervous system. The allelic and combinatorial expression of distinct variable exons of the Pcdha genes is a potential mechanism for specifying neuron identity in the brain.
引用
收藏
页码:171 / 176
页数:6
相关论文
共 27 条
  • [1] ALLELIC INACTIVATION REGULATES OLFACTORY RECEPTOR GENE-EXPRESSION
    CHESS, A
    SIMON, I
    CEDAR, H
    AXEL, R
    [J]. CELL, 1994, 78 (05) : 823 - 834
  • [2] PARENTAL IMPRINTING OF AUTOSOMAL MAMMALIAN GENES
    EFSTRATIADIS, A
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (02) : 265 - 280
  • [3] The cadherin-related neuronal receptor family: a novel diversified cadherin family at the synapse
    Hamada, S
    Yagi, T
    [J]. NEUROSCIENCE RESEARCH, 2001, 41 (03) : 207 - 215
  • [4] ALLELIC EXCLUSION OF LY49-FAMILY GENES ENCODING CLASS-I MHC-SPECIFIC RECEPTORS ON NK CELLS
    HELD, W
    ROLAND, J
    RAULET, DH
    [J]. NATURE, 1995, 376 (6538) : 355 - 358
  • [5] Diversity revealed by a novel family of cadherins expressed in neurons at a synaptic complex
    Kohmura, N
    Senzaki, K
    Hamada, S
    Kai, N
    Yasuda, R
    Watanabe, M
    Ishii, H
    Yasuda, M
    Mishina, M
    Yagi, T
    [J]. NEURON, 1998, 20 (06) : 1137 - 1151
  • [6] X-CHROMOSOMES AND DOSAGE COMPENSATION
    LYON, MF
    [J]. NATURE, 1986, 320 (6060) : 313 - 313
  • [7] Stochastic yet biased expression of multiple Dscam splice variants by individual cells
    Neves, G
    Zucker, J
    Daly, M
    Chess, A
    [J]. NATURE GENETICS, 2004, 36 (03) : 240 - 246
  • [8] From zebra stripes to postal zones: deciphering patterns of gene expression in the cerebellum
    Oberdick, J
    Baader, SL
    Schilling, K
    [J]. TRENDS IN NEUROSCIENCES, 1998, 21 (09) : 383 - 390
  • [9] CELLULAR LOCALIZATION OF IMMUNOGLOBULINS WITH DIFFERENT ALLOTYPIC SPECIFICITIES IN RABBIT LYMPHOID TISSUES
    PERNIS, B
    CHIAPPINO, G
    KELUS, AS
    GELL, PGH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1965, 122 (05) : 853 - +
  • [10] Phillips GR, 2003, J NEUROSCI, V23, P5096