Improvement of culture conditions and evidence for nuclear transformation by homologous recombination in a red alga, cyanidioschyzon merolae 10D

被引:165
作者
Minoda, A
Sakagami, R
Yagisawa, F
Kuroiwa, T
Tanaka, K
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Tokyo 1130032, Japan
[2] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Tokyo 1920392, Japan
[3] Rikkyo St Pauls Univ, Coll Sci, Dept Life Sci, Tokyo 1718501, Japan
[4] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, Tokyo 1130033, Japan
关键词
cultivation; Cyanidioschyzon merolae; 5-FOA resistance; homologous recombination; red algae; transformation;
D O I
10.1093/pcp/pch087
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Although the nuclear genome sequence of Cyanidioschyzon merolae 10D, a unicellular red alga, was recently determined, DNA transformation technology that is important as a model plant system has never been available thus far. In this study, improved culture conditions resulted in a faster growth rate of C. merolae in liquid medium (doubling time = 9.2 h), and colony formation on gellan gum plates. Using these conditions, spontaneous mutants (5-fluoroortic acid resistant) deficient in the UMP synthase gene were isolated. The lesions were then restored by introducing the wild-type UMP synthase gene into the cells suggesting DNA transformation by homologous recombination.
引用
收藏
页码:667 / 671
页数:5
相关论文
共 20 条
[1]   STUDIES WITH CYANIDIUM CALDARIUM, AN ANOMALOUSLY PIGMENTED CHLOROPHYTE [J].
ALLEN, MB .
ARCHIV FUR MIKROBIOLOGIE, 1959, 32 (03) :270-277
[2]  
BOEKE JD, 1987, METHOD ENZYMOL, V154, P164
[3]  
Harris EH, 1998, MOL BIOL CHLOROPLAST, P1
[4]  
Itoh R, 1997, EUR J CELL BIOL, V73, P252
[5]  
Kuroiwa T, 1998, BIOESSAYS, V20, P344, DOI 10.1002/(SICI)1521-1878(199804)20:4<344::AID-BIES11>3.3.CO
[6]  
2-L
[7]   Genome sequence of the ultrasmall unicellular red alga Cyanidioschyzon merolae 10D [J].
Matsuzaki, M ;
Misumi, O ;
Shin-I, T ;
Maruyama, S ;
Takahara, M ;
Miyagishima, SY ;
Mori, T ;
Nishida, K ;
Yagisawa, F ;
Nishida, K ;
Yoshida, Y ;
Nishimura, Y ;
Nakao, S ;
Kobayashi, T ;
Momoyama, Y ;
Higashiyama, T ;
Minoda, A ;
Sano, M ;
Nomoto, H ;
Oishi, K ;
Hayashi, H ;
Ohta, F ;
Nishizaka, S ;
Haga, S ;
Miura, S ;
Morishita, T ;
Kabeya, Y ;
Terasawa, K ;
Suzuki, Y ;
Ishii, Y ;
Asakawa, S ;
Takano, H ;
Ohta, N ;
Kuroiwa, H ;
Tanaka, K ;
Shimizu, N ;
Sugano, S ;
Sato, N ;
Nozaki, H ;
Ogasawara, N ;
Kohara, Y ;
Kuroiwa, T .
NATURE, 2004, 428 (6983) :653-657
[8]   HETEROSPECIFIC CLONING OF ARABIDOPSIS-THALIANA CDNAS BY DIRECT COMPLEMENTATION OF PYRIMIDINE AUXOTROPHIC MUTANTS OF SACCHAROMYCES-CEREVISIAE .1. CLONING AND SEQUENCE-ANALYSIS OF 2 CDNAS CATALYZING THE 2ND, 5TH AND 6TH STEPS OF THE DE-NOVO PYRIMIDINE BIOSYNTHESIS PATHWAY [J].
NASR, F ;
BERTAUCHE, N ;
DUFOUR, ME ;
MINET, M ;
LACROUTE, F .
MOLECULAR & GENERAL GENETICS, 1994, 244 (01) :23-32
[9]   The phylogenetic position of red algae revealed by multiple nuclear genes from mitochondria-containing eukaryotes and an alternative hypothesis on the origin of plastids [J].
Nozaki, H ;
Matsuzaki, M ;
Takahara, M ;
Misumi, O ;
Kuroiwa, H ;
Hasegawa, M ;
Shin-i, T ;
Kohara, Y ;
Ogasawara, N ;
Kuroiwa, T .
JOURNAL OF MOLECULAR EVOLUTION, 2003, 56 (04) :485-497
[10]   Molecular cloning and characterization of AtTERT, a telomerase reverse transcriptase homolog in Arabidopsis thaliana [J].
Oguchi, K ;
Liu, HT ;
Tamura, K ;
Takahashi, H .
FEBS LETTERS, 1999, 457 (03) :465-469