An antisense transcript to SMAD5 expressed in fetal and tumor tissues

被引:14
|
作者
Zavadil, J
Svoboda, P
Liang, H
Kottickal, LV
Nagarajan, L [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[2] Inst Hematol & Blood Transfus, Dept Cell Physiol, CR-12820 Prague, Czech Republic
关键词
D O I
10.1006/bbrc.1999.0256
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
SMAD5, a transducer of TGF-beta/BMP inhibitory signals and a tumor suppressor candidate, localizes to the region of invariant loss in human myeloid neoplasms, on chromosome 5q31.1. Recent evidence indicates a gene-dosage effect along the TGF-beta/BMP signaling pathways. We have identified a novel transcript. designated DAMS, whose 3' exonic sequences contain in part an alternate 5' exon of SMAD5, in the antisense orientation. Expressed sequenced tags (ESTs) for DAMS are found in fetal tissues (heart, adrenal glands, and total fetus) and pancreatic tumor cDNA libraries. In contrast to SMAD5, DAMS expression is not readily detectable in adult and fetal tissues. Semiquantitative PCR suggests that the stoichiometry between SMAD5 and DAMS transcripts ranges between 15 and 120 in normal and malignant hematopoietic cells. The findings raise the possibility that DAMS may be a fail-safe mechanism for precise regulation of SMAD5 transcript levels that may be critical in maintaining normal homeostasis. (C) 1999 Academic Press.
引用
收藏
页码:668 / 672
页数:5
相关论文
共 50 条
  • [21] SMAD5 as a novel gene for familial pulmonary arterial hypertension
    Cao, Ding
    Sirenko, Yuriy
    Radchenko, Ganna
    Gall, Henning
    Ahmed, Ayat
    Theiss, Susanne
    Haas, Simon
    Shaukat, Memoona
    Sassmannshausen, Zoe
    Benjamin, Nicola
    Xanthouli, Panagiota
    Harutyunova, Satenik
    Egenlauf, Benjamin
    Hinderhofer, Katrin
    Gruenig, Ekkehard
    Laugsch, Magdalena
    Eichstaedt, Christina
    EUROPEAN RESPIRATORY JOURNAL, 2023, 62
  • [22] Smad5 is required for mouse primordial germ cell development
    Chang, H
    Matzuk, MM
    MECHANISMS OF DEVELOPMENT, 2001, 104 (1-2) : 61 - 67
  • [23] Mitochondrial localization of Smad5 in a human chondrogenic cell line
    Jüllig, M
    Stott, NS
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 307 (01) : 108 - 113
  • [24] Conditional deletion of Smad1 and Smad5 in somatic cells of male and female gonads leads to metastatic tumor development in mice
    Pangas, Stephanie A.
    Li, Xiaohui
    Umans, Lieve
    Zwijsen, An
    Huylebroeck, Danny
    Gutierrez, Carolina
    Wang, Degang
    Martin, James F.
    Jamin, Soazik P.
    Behringer, Richard R.
    Robertson, Elizabeth J.
    Matzuk, Martin M.
    MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (01) : 248 - 257
  • [25] Smad5 is essential for left-right asymmetry in mice
    Chang, H
    Zwijsen, A
    Vogel, H
    Huylebroeck, D
    Matzuk, MM
    DEVELOPMENTAL BIOLOGY, 2000, 219 (01) : 71 - 78
  • [26] BMP canonical Smad signaling through Smad1 and Smad5 is required for endochondral bone formation
    Retting, Kelsey N.
    Song, Buer
    Yoon, Byeong S.
    Lyons, Karen M.
    DEVELOPMENT, 2009, 136 (07): : 1093 - 1104
  • [27] Smad5 Haploinsufficiency Leads to Hair Cell and Hearing Loss
    Yang, Shi-Ming
    Guo, Wei-Wei
    Hu, Yin-Yan
    Sun, Yan-Xun
    Hou, Zhao-Hui
    Sun, Jian-He
    Wang, Xiang
    He, David Z. Z.
    Zhai, Suo-Qiang
    Young, Wie-Yen
    Han, Dong-Yi
    Yang, Xiao
    DEVELOPMENTAL NEUROBIOLOGY, 2009, 69 (2-3) : 153 - 161
  • [28] BMP4/Smad5 dependent stress erythropoiesis is required for the expansion of erythroid progenitors during fetal development
    Porayette, Prashanth
    Paulson, Robert F.
    DEVELOPMENTAL BIOLOGY, 2008, 317 (01) : 24 - 35
  • [29] Nuclear SMAD5 dances to a different tune in regulating insulin secretion
    Orlowski, John
    CELL METABOLISM, 2024, 36 (06) : 1169 - 1171
  • [30] Spatio-temporal activation of Smad1 and Smad5 in vivo: monitoring transcriptional activity of Smad proteins
    Monteiro, RM
    Lopes, SMCD
    Korchynskyi, O
    ten Dijke, P
    Mummery, CL
    JOURNAL OF CELL SCIENCE, 2004, 117 (20) : 4653 - 4663