Isolation of the human BACH1 transcription regulator gene, which maps to chromosome 21q22.1

被引:0
|
作者
Jean-Louis Blouin
Geneviève Duriaux Saïl
Michel Guipponi
Colette Rossier
Marie-Pierre Pappasavas
S. E. Antonarakis
机构
[1] Division of Medical Genetics,
[2] Centre Médical Universitaire,undefined
[3] 1 rue Michel Servet,undefined
[4] CH-1211 Genève,undefined
[5] Switzerland Tel.: +41-22-702-5707; Fax: +41-22-702-5706; e-mail: Stylianos.Antonarakis@medecine.unige.ch,undefined
[6] Laboratory of Human Molecular Genetics,undefined
[7] Department of Genetics and Microbiology,undefined
[8] University of Geneva Medical School,undefined
[9] Geneva,undefined
[10] Switzerland,undefined
来源
Human Genetics | 1998年 / 102卷
关键词
Leucine Zipper; mRNA Species; Yeast Artificial Chromosome; Monogenic Disorder; Transcription Regulator Gene;
D O I
暂无
中图分类号
学科分类号
摘要
In order to contribute to the development of the transcriptional map of chromosome 21, we performed exon trapping using cosmid clones mapped in the region 21q22.1–22.2 and identified a number of potential exons. One of the trapped exons (Genbank No. AF026200) showed a strong homology with the mouse Bach1 gene (Genbank No. D86603), a transcription factor regulating gene expression. We then isolated the full-length coding region of the human BACH1 gene using expressed sequence tags, reverse transcription-polymerase chain reaction and rapid amplification of cDNA ends. The predicted BACH1 protein contains 736 amino acids and is 88% identical to its mouse homolog. It contains basic leucine zipper and BTB-zinc finger domains (which are directly involved in DNA binding for transcription regulation). The BACH1 gene maps in a relatively gene-poor region on 21q22.1 in yeast artificial chromosome 814c1 of the collection of Chumakov et al. Northern blot analysis revealed that it is expressed as an mRNA species of approximately 5.8 kb in all 16 adult and 4 fetal tissues examined; an additional mRNA species of 2.8 kb was observed in adult testis. The contribution of the BACH1 gene to the pathophysiology of trisomy or monosomy 21 is unknown. In addition, no monogenic disorders associated with mutations in the BACH1 gene have yet been identified.
引用
收藏
页码:282 / 288
页数:6
相关论文
共 50 条
  • [31] Cyclin T2A gene maps on human chromosome 2q21
    De Luca, A
    Tosolini, A
    Russo, P
    Severino, A
    Baldi, A
    De Luca, L
    Cavallotti, I
    Baldi, F
    Giordano, A
    Testa, JR
    Paggi, MG
    JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2001, 49 (06) : 693 - 697
  • [32] PKNOX1, a gene encoding PREP1, a new regulator of PBX activity, maps on human chromosome 21q22.3 and murine chromosome 17B/C
    Berthelsen, J
    Viggiano, L
    Schulz, H
    Ferretti, E
    Consalez, GG
    Rocchi, M
    Blasi, F
    GENOMICS, 1998, 47 (02) : 323 - 324
  • [33] The B-lymphocyte maturation promoting transcription factor BLIMP1/PRDI-BF1 maps to D6S447 on human chromosome 6q21-q22.1 and the syntenic region of mouse chromosome 10
    Mock, BA
    Liu, LM
    LePaslier, D
    Huang, S
    GENOMICS, 1996, 37 (01) : 24 - 28
  • [34] hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia
    Gerald Stöber
    Jobst Meyer
    Indrajit Nanda
    Thomas F. Wienker
    Kathrin Saar
    Susanne Jatzke
    Michael Schmid
    Klaus-Peter Lesch
    Helmut Beckmann
    European Archives of Psychiatry and Clinical Neuroscience, 2000, 250 : 163 - 168
  • [35] Cloning of human Bach1 transcription factor which regulates transcription through NF-E2 site with small Maf proteins.
    Toki, T
    Kanezaki, R
    Arai, K
    Yokoyama, M
    Igarashi, K
    Yamamoto, M
    Ito, E
    BLOOD, 1997, 90 (10) : 196 - 196
  • [36] hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia
    Stöber, G
    Meyer, J
    Nanda, I
    Wienker, TF
    Saar, K
    Jatzke, S
    Schmid, M
    Lesch, KP
    Beckmann, H
    EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2000, 250 (04) : 163 - 168
  • [37] Characterization of a human homolog (OVOL1) of the Drosophila ovo gene, which maps to Chromosome 11q13
    A. Chidambaram
    R. Allikmets
    S. Chandrasekarappa
    S. C. Guru
    W. Modi
    B. Gerrard
    M. Dean
    Mammalian Genome, 1997, 8 : 950 - 951
  • [38] Characterization of a human homolog (OVOL1) of the Drosophila ovo gene, which maps to Chromosome 11q13
    Chidambaram, A
    Allikmets, R
    Chandrasekarappa, S
    Guru, SC
    Modi, W
    Gerrard, B
    Dean, M
    MAMMALIAN GENOME, 1997, 8 (12) : 950 - 951
  • [39] Structure and expression of Strabismus 1 gene on human chromosome 1q21-q23
    Katoh, M
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2002, 20 (06) : 1197 - 1203
  • [40] The novel epithelial-specific Ets transcription factor gene ESX maps to human chromosome 1q32.1
    Oettgen, P
    Carter, KC
    Augustus, M
    Barcinski, M
    Boltax, J
    Kunsch, C
    Libermann, TA
    GENOMICS, 1997, 45 (02) : 456 - 457