Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2001-11-19
pubmed:abstractText
Two chlorophyll-deficient mutants of Chlamydomonas reinhardtii, chl1 and brs-1, are light sensitive and, when grown heterotrophically in the dark, accumulate protoporphyrin IX and exhibit yellow/orange pigmentation. The lesions in both mutants were mapped to the gene (CHLH) for the plastid-localized H subunit of the heterotrimeric magnesium chelatase that catalyzes the insertion of magnesium into protoporphyrin IX. The genetic defects in the mutants could be assigned to +1 frameshift mutations in exon 9 (chl1) and exon 10 (brs-1) of the CHLH gene. In both mutants, the H subunit of magnesium chelatase was undetectable, but, as shown for chl1, the steady-state levels of the I and D subunits were unaltered in comparison to wild type. The CHLH gene exhibits marked light inducibility: levels of both the mRNA and the protein product are strongly increased when cultures are shifted from from the dark into the light, suggesting that this protein may play a crucial role in the light regulation of chlorophyll biosynthesis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aminolevulinic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins, http://linkedlifedata.com/resource/pubmed/chemical/CHL1 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Carboxypeptidases, http://linkedlifedata.com/resource/pubmed/chemical/ChlH protein, Synechocystis, http://linkedlifedata.com/resource/pubmed/chemical/Chlorophyll, http://linkedlifedata.com/resource/pubmed/chemical/Chromosomal Proteins, Non-Histone, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lyases, http://linkedlifedata.com/resource/pubmed/chemical/Methyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Porphyrins, http://linkedlifedata.com/resource/pubmed/chemical/Protoporphyrins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/magnesium chelatase, http://linkedlifedata.com/resource/pubmed/chemical/protoporphyrinogen, http://linkedlifedata.com/resource/pubmed/chemical/serine carboxypeptidase
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1617-4615
pubmed:author
pubmed:issnType
Print
pubmed:volume
266
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
363-73
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11713666-Amino Acid Sequence, pubmed-meshheading:11713666-Aminolevulinic Acid, pubmed-meshheading:11713666-Animals, pubmed-meshheading:11713666-Bacterial Proteins, pubmed-meshheading:11713666-Blotting, Southern, pubmed-meshheading:11713666-Blotting, Western, pubmed-meshheading:11713666-Carboxypeptidases, pubmed-meshheading:11713666-Chlamydomonas, pubmed-meshheading:11713666-Chlorophyll, pubmed-meshheading:11713666-Chloroplasts, pubmed-meshheading:11713666-Chromosomal Proteins, Non-Histone, pubmed-meshheading:11713666-Cloning, Molecular, pubmed-meshheading:11713666-DNA Primers, pubmed-meshheading:11713666-Frameshift Mutation, pubmed-meshheading:11713666-Fungal Proteins, pubmed-meshheading:11713666-Genetic Complementation Test, pubmed-meshheading:11713666-Lyases, pubmed-meshheading:11713666-Methyltransferases, pubmed-meshheading:11713666-Molecular Sequence Data, pubmed-meshheading:11713666-Polymerase Chain Reaction, pubmed-meshheading:11713666-Porphyrins, pubmed-meshheading:11713666-Protoporphyrins, pubmed-meshheading:11713666-RNA, Messenger, pubmed-meshheading:11713666-Saccharomyces cerevisiae Proteins
pubmed:year
2001
pubmed:articleTitle
Characterization of Chlamydomonas mutants defective in the H subunit of Mg-chelatase.
pubmed:affiliation
Institut für Biologie III, Universität Freiburg, Schänzlestrasse 1, 79104 Freiburg, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't