Literature DB >> 16059773

Identification of novel cAMP responsive element modulator (CREM) isoforms expressed by osteoblasts.

F Liu1, Y-F Huang, B E Kream.   

Abstract

CREM, the cyclic adenosine monophosphate (cAMP) responsive element modulator, belongs to a multigene family of cAMP-responsive transcription factors. CREM encodes a variety of different isoforms by utilizing four promoters and a complex pattern of alternative messenger ribonucleic acid (mRNA) splicing. We showed previously that parathyroid hormone induces the CREM P2 promoter products known as ICER (inducible cAMP early repressor) in osteoblasts. Herein we report that osteoblasts also express at least 15 CREM transcripts initiated from the P1 promoter, including 7 novel transcripts that result from alternative splicing. It is of interest that we found that CREM-X contains both exon theta1, previously identified only in P3 promoter products, and a new exon termed L, which is located upstream of exon theta1.

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Year:  2005        PMID: 16059773     DOI: 10.1007/s00223-005-0003-1

Source DB:  PubMed          Journal:  Calcif Tissue Int        ISSN: 0171-967X            Impact factor:   4.333


  3 in total

1.  CREM deficiency in mice alters the response of bone to intermittent parathyroid hormone treatment.

Authors:  Fei Liu; Sun-Kyeong Lee; Douglas J Adams; Gloria A Gronowicz; Barbara E Kream
Journal:  Bone       Date:  2007-02-01       Impact factor: 4.398

2.  Family members CREB and CREM control thyrotropin-releasing hormone (TRH) expression in the hypothalamus.

Authors:  Franck Chiappini; Preeti Ramadoss; Kristen R Vella; Lucas L Cunha; Felix D Ye; Ronald C Stuart; Eduardo A Nillni; Anthony N Hollenberg
Journal:  Mol Cell Endocrinol       Date:  2012-09-20       Impact factor: 4.102

3.  Calcitonin induces expression of the inducible cAMP early repressor in osteoclasts.

Authors:  Maobin Yang; Barbara E Kream
Journal:  Endocrine       Date:  2008-06       Impact factor: 3.633

  3 in total

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