Literature DB >> 10654256

Evolution of cis-acting elements in 5' flanking regions of vertebrate actin genes.

T Liu1, J Wu, F He.   

Abstract

Regulation of the vertebrate actin multigene family involves the recognition of various regulatory sequences (cis-acting elements) that specify the distinct tissue type and developmental program of expression for each actin paralogue, which implies that the distribution of cis-acting elements may be unique for each paralogue gene. To elucidate the evolution of these unique distribution patterns, we improved a method to scan for cis-acting elements in the 5' flanking regulatory region of genes and used it to analyze five cis-acting elements (SRE, MyoD binding site, Elk-1 binding site, positive and negative YY1 binding sites) of six actin paralogue genes (beta and gamma cytoplasmic actins, alpha and gamma smooth muscle actins, and alpha skeletal and alpha cardiac actins) among various vertebrates. It was shown that although an element(s) may exist in all paralogue genes of the same species, its numbers, compositions, and distribution patterns or even sequences vary remarkably among paralogues, which contributes to their different tissue- and developmental-specific expression. However, each pair of coexpressed paralogues has some certain similarity in distribution patterns. Furthermore, among various orthologues of actin genes derived from diverse vertebrates, the sequences, numbers, and distribution patterns of these cis-acting elements are highly conserved or even identical in the long run of phylogeny of vertebrates. Taken together, the results described above strongly indicate that not only the structures of actins but also their expression patterns are essential in both the phylogeny and the physiology of vertebrates. The distribution patterns of cis-acting elements of various actin genes can be regarded as indicators of both horizontal (paralogues) and vertical (orthologous) evolution of actins.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10654256     DOI: 10.1007/s002399910003

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  6 in total

1.  Evolution of functionally conserved enhancers can be accelerated in large populations: a population-genetic model.

Authors:  Ashley J R Carter; Günter P Wagner
Journal:  Proc Biol Sci       Date:  2002-05-07       Impact factor: 5.349

2.  Effects of random mutations in the human immunodeficiency virus type 1 transcriptional promoter on viral fitness in different host cell environments.

Authors:  Tim van Opijnen; Maarten C Boerlijst; Ben Berkhout
Journal:  J Virol       Date:  2006-07       Impact factor: 5.103

3.  Cytoplasmic YY1 is associated with increased smooth muscle-specific gene expression: implications for neonatal pulmonary hypertension.

Authors:  Laure Favot; Susan M Hall; Sheila G Haworth; Paul R Kemp
Journal:  Am J Pathol       Date:  2005-12       Impact factor: 4.307

4.  Increased actin polymerization reduces the inhibition of serum response factor activity by Yin Yang 1.

Authors:  Peter D Ellis; Karen M Martin; Colin Rickman; James C Metcalfe; Paul R Kemp
Journal:  Biochem J       Date:  2002-06-01       Impact factor: 3.857

5.  Transcription of muscle actin genes by a nuclear form of mitochondrial RNA polymerase.

Authors:  Yu-Ling Lee; Chun-Hui Chiao; Ming-Ta Hsu
Journal:  PLoS One       Date:  2011-07-25       Impact factor: 3.240

6.  Binding of serum response factor to cystic fibrosis transmembrane conductance regulator CArG-like elements, as a new potential CFTR transcriptional regulation pathway.

Authors:  Céline René; Magali Taulan; Florence Iral; Julien Doudement; Aurore L'Honoré; Catherine Gerbon; Jacques Demaille; Mireille Claustres; Marie-Catherine Romey
Journal:  Nucleic Acids Res       Date:  2005-09-16       Impact factor: 16.971

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.