Literature DB >> 2022339

Transcriptional regulatory elements in the 5' upstream and first intron regions of the human smooth muscle (aortic type) alpha-actin-encoding gene.

Y Nakano1, T Nishihara, S Sasayama, T Miwa, S Kamada, T Kakunaga.   

Abstract

We have determined the nucleotide (nt) sequence of 5.5 kb including the 5' flanking, first untranslated exon and first intron regions of the human smooth muscle (SM) (aortic type) alpha-actin-(Sm alpha A)- encoding gene. The promoter region and a part of the first intron show remarkably high sequence conservation with equivalent regions of the chicken gene, and contain multiple transcriptional regulatory elements. From transient chloramphenicol acetyltransferase gene (cat) expression assays in SM cells, a DNA fragment from nt -123 to +49 containing two CArG boxes showed strong positive promoter activity, whereas a far upstream region from nt -253 to -124 showed a negative effect. The conserved region in the first intron also contains the CArG box and showed an enhancer activity. Therefore, the human SM alpha A gene is controlled under positive and negative mechanisms.

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Year:  1991        PMID: 2022339     DOI: 10.1016/0378-1119(91)90140-7

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  8 in total

1.  Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene: evolution of six human actin genes.

Authors:  T Miwa; Y Manabe; K Kurokawa; S Kamada; N Kanda; G Bruns; H Ueyama; T Kakunaga
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

Review 2.  An analysis of vertebrate mRNA sequences: intimations of translational control.

Authors:  M Kozak
Journal:  J Cell Biol       Date:  1991-11       Impact factor: 10.539

3.  Cell-specific transcription of the smooth muscle gamma-actin gene requires both positive- and negative-acting cis elements.

Authors:  A M Kovacs; W E Zimmer
Journal:  Gene Expr       Date:  1998

4.  Glioblastoma stem cells generate vascular pericytes to support vessel function and tumor growth.

Authors:  Lin Cheng; Zhi Huang; Wenchao Zhou; Qiulian Wu; Shannon Donnola; James K Liu; Xiaoguang Fang; Andrew E Sloan; Yubin Mao; Justin D Lathia; Wang Min; Roger E McLendon; Jeremy N Rich; Shideng Bao
Journal:  Cell       Date:  2013-03-28       Impact factor: 41.582

5.  Facilitated hyperpolarization signaling in vascular smooth muscle-overexpressing TRIC-A channels.

Authors:  Shengchen Tao; Daiju Yamazaki; Shinji Komazaki; Chengzhu Zhao; Tsunaki Iida; Sho Kakizawa; Yuji Imaizumi; Hiroshi Takeshima
Journal:  J Biol Chem       Date:  2013-04-16       Impact factor: 5.157

6.  Targeting myofibroblasts in model systems of fibrosis by an artificial alpha-smooth muscle-actin promoter hybrid.

Authors:  Julia Hirschfeld; Julia Maurer; Diana Jung; Monika Kwiecinski; Al Karim Khimji; Hans Peter Dienes; Jochen W U Fries; Margarete Odenthal
Journal:  Mol Biotechnol       Date:  2009-06-24       Impact factor: 2.695

7.  Human functional genetic studies are biased against the medically most relevant primate-specific genes.

Authors:  Lili Hao; Xiaomeng Ge; Haolei Wan; Songnian Hu; Martin J Lercher; Jun Yu; Wei-Hua Chen
Journal:  BMC Evol Biol       Date:  2010-10-20       Impact factor: 3.260

8.  Skeletal myosin heavy chain function in cultured lung myofibroblasts.

Authors:  Nancy A Rice; Leslie A Leinwand
Journal:  J Cell Biol       Date:  2003-10-13       Impact factor: 10.539

  8 in total

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