A comprehensive transcript map of the mouse Gnas imprinted complex

被引:48
作者
Holmes, R
Williamson, C
Peters, J
Denny, P
Wells, C [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] MRC, Mammalian Genet Unit, Harwell OX11 0RD, Berks, England
[3] RIKEN, Yokohama Inst, Gen Sci Ctr, Lab Genome Explorat,Res Grp,Tsurumi Ku, Kanagawa 2300045, Japan
[4] RIKEN, Genome Sci Lab, Wako, Saitama 3510198, Japan
关键词
D O I
10.1101/gr.955503
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The recent publication of the FANTOM mouse transcriptome has provided a unique opportunity to study the diversity of transcripts arising from a single gene locus. We have focused on the Gnas complex, as imprinting loci themselves provide unique insights into transcriptional regulation. Thirteen full-length cDNAs from the FANTOM2 set were mapped to the Gnas locus. These represented one previously described transcript and 12 putative new transcripts. Of these, eight were found to be differentially expressed from either the maternal or paternal allele. Two clones extended Nespas in the 3' direction, providing evidence of antisense transcription spanning a 30-kb genomic region from a single allele. The transcripts were summarized into six transcriptional units, Nespas, Nesp, Gnasxl, F7, exon 1A, and Gnas. The resolution of the Gnas transcript map by the FANTOM2 clones revealed a pattern of alternate splicing. In addition to the transcripts described previously as splicing onto exon 2 of Gnas, each new sense transcript had an alternate short 3'UTR independent of Gnas. Both spliced and unspliced variants of the new imprinted sense transcripts were found. Whereas the functional significance of these alternate transcripts is not known, the availability of the FANTOM clones has provided remarkable insights into the repertoire of transcripts in the Gnas complex locus.
引用
收藏
页码:1410 / 1415
页数:6
相关论文
共 24 条
  • [1] Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13
    Bonthron, DT
    Hayward, BE
    Moran, V
    Strain, L
    [J]. HUMAN GENETICS, 2000, 107 (02) : 165 - 175
  • [2] Two imprinted gene mutations: three phenotypes
    Cattanach, BM
    Peters, J
    Ball, S
    Rasberry, C
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (15) : 2263 - 2273
  • [3] DIFFERENTIAL ACTIVITY OF MATERNALLY AND PATERNALLY DERIVED CHROMOSOME REGIONS IN MICE
    CATTANACH, BM
    KIRK, M
    [J]. NATURE, 1985, 315 (6019) : 496 - 498
  • [4] GENOMIC SEQUENCING
    CHURCH, GM
    GILBERT, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07): : 1991 - 1995
  • [5] CRAWFORD JA, 1993, J BIOL CHEM, V268, P9879
  • [6] An imprinted antisense transcript at the human GNAS1 locus
    Hayward, BE
    Bonthron, DT
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (05) : 835 - 841
  • [7] The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins
    Hayward, BE
    Kamiya, M
    Strain, L
    Moran, V
    Campbell, R
    Hayashizaki, Y
    Bonthron, DT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) : 10038 - 10043
  • [8] Identification of imprinted loci by methylation-sensitive representational difference analysis: Application to mouse distal chromosome 2
    Kelsey, G
    Bodle, D
    Miller, HJ
    Beechey, CV
    Coombes, C
    Peters, J
    Williamson, CM
    [J]. GENOMICS, 1999, 62 (02) : 129 - 138
  • [9] Disruption of imprinted X inactivation by parent-of-origin effects at Tsix
    Lee, JT
    [J]. CELL, 2000, 103 (01) : 17 - 27
  • [10] Tissue-specific expression of antisense and sense transcripts at the imprinted Gnas locus
    Li, T
    Vu, TH
    Zeng, ZL
    Nguyen, BT
    Hayward, BE
    Bonthron, DT
    Hu, JF
    Hoffman, AR
    [J]. GENOMICS, 2000, 69 (03) : 295 - 304