TY - JOUR
T1 - Molecular map of the Chlamydomonas reinhardtii nuclear genome
AU - Kathir, Pushpa
AU - LaVoie, Matthew
AU - Brazelton, William J.
AU - Haas, Nancy A.
AU - Lefebvre, Paul A.
AU - Silflow, Carolyn D.
PY - 2003/4
Y1 - 2003/4
N2 - We have prepared a molecular map of the Chlamydomonas reinhardtii genome anchored to the genetic map. The map consists of 264 markers, including sequence-tagged sites (STS), scored by use of PCR and agarose gel electrophoresis, and restriction fragment length polymorphism markers, scored by use of Southern blot hybridization. All molecular markers tested map to one of the 17 known linkage groups of C. reinhardtii. The map covers approximately 1,000 centimorgans (cM). Any position on the C. reinhardtii genetic map is, on average, within 2 cM of a mapped molecular marker. This molecular map, in combination with the ongoing mapping of bacterial artificial chromosome (BAC) clones and the forthcoming sequence of the C. reinhardtii nuclear genome, should greatly facilitate isolation of genes of interest by using positional cloning methods. In addition, the presence of easily assayed STS markers on each arm of each linkage group should be very useful in mapping new mutations in preparation for positional cloning.
AB - We have prepared a molecular map of the Chlamydomonas reinhardtii genome anchored to the genetic map. The map consists of 264 markers, including sequence-tagged sites (STS), scored by use of PCR and agarose gel electrophoresis, and restriction fragment length polymorphism markers, scored by use of Southern blot hybridization. All molecular markers tested map to one of the 17 known linkage groups of C. reinhardtii. The map covers approximately 1,000 centimorgans (cM). Any position on the C. reinhardtii genetic map is, on average, within 2 cM of a mapped molecular marker. This molecular map, in combination with the ongoing mapping of bacterial artificial chromosome (BAC) clones and the forthcoming sequence of the C. reinhardtii nuclear genome, should greatly facilitate isolation of genes of interest by using positional cloning methods. In addition, the presence of easily assayed STS markers on each arm of each linkage group should be very useful in mapping new mutations in preparation for positional cloning.
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U2 - 10.1128/EC.2.2.362-379.2003
DO - 10.1128/EC.2.2.362-379.2003
M3 - Article
C2 - 12684385
AN - SCOPUS:0038058753
SN - 1535-9778
VL - 2
SP - 362
EP - 379
JO - Eukaryotic Cell
JF - Eukaryotic Cell
IS - 2
ER -