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PMID: 17872446 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Functional architecture and evolution of transcriptional elements that drive gene coexpression.

Science (New York, N.Y.) ·Vol. 317 ·No. 5844 ·2007-09-14 ·Pages 1557-60

Brown CD, Johnson DS, Sidow A

Abstract

Transcriptional coexpression of interacting gene products is required for complex molecular processes; however, the function and evolution of cis-regulatory elements that orchestrate coexpression remain largely unexplored. We mutagenized 19 regulatory elements that drive coexpression of Ciona muscle genes and obtained quantitative estimates of the cis-regulatory activity of the 77 motifs that comprise these elements. We found that individual motif activity ranges broadly within and among elements, and among different instantiations of the same motif type. The activity of orthologous motifs is strongly constrained, although motif arrangement, type, and activity vary greatly among the elements of different co-regulated genes. Thus, the syntactical rules governing this regulatory function are flexible but become highly constrained evolutionarily once they are established in a particular element.

MeSH Terms
Animals Ciona intestinalis/embryology,genetics Creatine Kinase/genetics Embryo, Nonmammalian/metabolism Evolution, Molecular Gene Expression Regulation, Developmental Muscle Proteins/genetics Muscles/cytology,embryology,metabolism Mutation Regulatory Sequences, Nucleic Acid Response Elements Selection, Genetic Transcription, Genetic Urochordata/embryology,genetics
Chemicals
Muscle Proteins Creatine Kinase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brown Christopher D
Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Johnson David S
Sidow Arend
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2007-09-14
Pages
1557-60
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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