Single mutations in sas A enable a simpler δcikA gene network architecture with equivalent circadian properties

Proceedings of the National Academy of Sciences of the United States of America

Volumn 111, Issue 47, 2014, Pages E5069-E5075

  Shultzaberger, Ryan K ^a,b   Boyd, Joseph S ^a   Katsuki, Takeo ^b   Golden, Susan S ^a   Greenspan, Ralph J ^a,b  

^a San Diego   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cyanobacteria; Evolution; Gene network

Indexed keywords

CIRCADIAN INPUT KINASE A; GENOMIC DNA; PROTEIN KINASE; UNCLASSIFIED DRUG; BACTERIAL PROTEIN; CIKA PROTEIN, BACTERIA;

ARTICLE; CIKA GENE; CIRCADIAN RHYTHM; CYANOBACTERIUM; GENE; GENE MUTATION; GENE REGULATORY NETWORK; GENOME; MUTAGENESIS; NONHUMAN; PHENOTYPE; SASA GENE; SYNECHOCOCCUS ELONGATUS; BACTERIAL GENE; GENETIC POLYMORPHISM; GENETICS; POINT MUTATION; SYNECHOCOCCUS;

CYANOBACTERIA; SASA; SYNECHOCOCCUS; SYNECHOCOCCUS ELONGATUS; SYNECHOCOCCUS ELONGATUS PCC 6301; SYNECHOCOCCUS ELONGATUS PCC 7942;

BACTERIAL PROTEINS; CIRCADIAN RHYTHM; GENE REGULATORY NETWORKS; GENES, BACTERIAL; POINT MUTATION; POLYMORPHISM, GENETIC; PROTEIN KINASES; SYNECHOCOCCUS;

EID: 85047699273     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1419902111     Document Type: Article

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