Identification of a novel bone morphogenetic protein (BMP)-inducible transcript, BMP-inducible transcript-1, by utilizing the conserved BMP-responsive elements in the Id genes.

Bone morphogenetic proteins (BMPs) inhibit myogenesis and induce osteoblastic differentiation in myoblasts. They also induce the transcription of several common genes, such as Id1, Id2 and Id3, in various cell types. We have reported that a GC-rich element in the Id1 gene functions as a BMP-responsi...

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Publicado en:Journal of Bone & Mineral Metabolism Vol. 31; no. 1; pp. 34 - 44
Autores principales: Shin M, Ohte S, Fukuda T, Sasanuma H, Yoneyama K, Kokabu S, Miyamoto A, Tsukamoto S, Hohjoh H, Jimi E, Katagiri T, Shin, Masashi, Ohte, Satoshi, Fukuda, Toru, Sasanuma, Hiroki, Yoneyama, Katsumi, Kokabu, Shoichiro, Miyamoto, Arei, Tsukamoto, Sho, Hohjoh, Hirohiko
Formato: research Journal Article
Publicado: Springer Nature Jan2013
Acceso en línea:Ver este registro en EBSCOhost
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        09148779
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      jtl: Journal of Bone & Mineral Metabolism
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      dt: Jan2013
      vid: 31
      iid: 1
      pid: 237
      pub: Springer Nature
      place: New York, New York
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        104294807
        NLM22976053
        2011900167
        10.1007/s00774-012-0381-1
        NLM22976053
        104294807
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        atl: Identification of a novel bone morphogenetic protein (BMP)-inducible transcript, BMP-inducible transcript-1, by utilizing the conserved BMP-responsive elements in the Id genes.
      aug:
        au:
          Shin M
          Ohte S
          Fukuda T
          Sasanuma H
          Yoneyama K
          Kokabu S
          Miyamoto A
          Tsukamoto S
          Hohjoh H
          Jimi E
          Katagiri T
          Shin, Masashi
          Ohte, Satoshi
          Fukuda, Toru
          Sasanuma, Hiroki
          Yoneyama, Katsumi
          Kokabu, Shoichiro
          Miyamoto, Arei
          Tsukamoto, Sho
          Hohjoh, Hirohiko
        affil: Division of Pathophysiology, Research Center for Genomic Medicine, Saitama Medical University, 1397-1 Yamane, Hidaka-shi, Saitama, 350-1241, Japan
      sug:
        subj:
          Bone Morphogenetic Proteins Metabolism
          DNA Physiology
          Muscle Proteins Metabolism
          Proteins
          RNA Metabolism
          Signal Transduction Physiology
          Stem Cells Metabolism
          Animal Studies
          Bone Morphogenetic Proteins
          Cells
          Chromosomes
          Chromosomes Metabolism
          Immunity
          Mice
          Muscle Proteins
          RNA
      ab: Bone morphogenetic proteins (BMPs) inhibit myogenesis and induce osteoblastic differentiation in myoblasts. They also induce the transcription of several common genes, such as Id1, Id2 and Id3, in various cell types. We have reported that a GC-rich element in the Id1 gene functions as a BMP-responsive element (BRE) that is regulated by Smads. In this study, we analyzed and identified BREs in the 5'-flanking regions of the mouse Id2 and Id3 genes. The core GGCGCC sequence was conserved among the BREs in the Id1, Id2 and Id3 genes and was essential for the response to BMP signaling via Smads. We found a novel BRE on mouse chromosome 13 at position 47,723,740-47,723,768 by searching for conserved sequences containing the Id1 BRE. This potential BRE was found in the 5'-flanking region of a novel gene that produces a non-coding transcript, termed BMP-inducible transcript-1 (BIT-1), and this element regulated the expression of this gene in response to BMP signaling. We found that BIT-1 is expressed in BMP target tissues such as the testis, brain, kidney and cartilage. These findings suggest that the transcriptional induction of the Ids, BIT-1 and additional novel genes containing the conserved BRE sequence may play an important role in the regulation of the differentiation and/or function of target cells in response to BMPs.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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        islocal: N