新疆大学生命科学与技术学院,新疆大学生命科学与技术学院,新疆大学生命科学与技术学院,新疆大学生命科学与技术学院,俄罗斯圣比得堡国立大学遗传与育种学教研室 乌鲁木齐830046,乌鲁木齐830046,乌鲁木齐830046,乌鲁木齐830046,圣比得堡,199034
纸质出版:2006
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[1]吾甫尔·米吉提,艾山江·阿布都拉,徐琴,等.莱茵衣藻(Chlamydomonas reinhardtii)cbn1和cao突变基因的对比分析及CAO基因的分子定位[J].新疆大学学报(自然科学版),2006(04):384-388.
吾甫尔·米吉提, 艾山江·阿布都拉, 徐琴, et al. 莱茵衣藻(Chlamydomonasreinhardtii)cbn1和cao突变基因的对比分析及CAO基因的分子定位[J]. Journal of Xinjiang University (Natural Science Edition in Chinese and English), 2006, (4).
[1]吾甫尔·米吉提,艾山江·阿布都拉,徐琴,等.莱茵衣藻(Chlamydomonas reinhardtii)cbn1和cao突变基因的对比分析及CAO基因的分子定位[J].新疆大学学报(自然科学版),2006(04):384-388. DOI:
吾甫尔·米吉提, 艾山江·阿布都拉, 徐琴, et al. 莱茵衣藻(Chlamydomonasreinhardtii)cbn1和cao突变基因的对比分析及CAO基因的分子定位[J]. Journal of Xinjiang University (Natural Science Edition in Chinese and English), 2006, (4). DOI:
用电击法将带有CAO基因片段的P sp109-E 8质粒转入到莱茵衣藻cbn1-48m t+基因突变株中后
转化子中出现了叶绿素b的恢复性表达
初步验证了丧失合成叶绿素b能力的cbn1和cao突变基因具有等位性的属性;将1641-1b(cbn1-43 m t+)和CC-1354(cbn1-48 m t+)突变株分别与CBS5(cao5 m t-)突变株的分离子CBS5-c1和CBS5-c5进行杂交
并通过随机分析方法分离获得1842个减数分裂后代分离子
经检测其中均没有发现有野生性表型的分离子
初步证明cbn1和cao 4突变基因间有着非常紧密的连锁性;从上述杂交系分离获得的50多个四分子中也没有检测发现显示野生性表型的分离子
进一步证明了cbn1和cao突变基因具有等位性的属性;根据CAO基因的DNA序列
从5′-端和3′-端设计两个探针
分别与莱茵衣藻核基因组Ⅰ号染色体上GBP 1和RB 47分子标记之间的21个BAC克隆进行的点杂交实验结果显示
该两个探针序列与21号BAC克隆(莱茵衣藻BAC文库序列号33e2)片段均有同源区的特性
此项DNA杂交实验初步证明
CAO基因的位点是在cbn1突变基因左右两侧的GBP 1和RB 47两个分子标记之间的33e2 BAC克隆片段区.
The plasmid PSP109-E8 containing CAO was transformed into Chlamydomonas cbn1-48 mt+ mutant strian by electroporation.And the recovery expression of the chlorophyll b was detected in transformants
the result indicated that the mutant genes cbn1 and cao which both lost the ability of chlorophyll b synthesis have allelic characters;1641-1b(cbn1-43 mt+)and CC-1354(cbn1-48 mt+) mutant strains were taken mating with the CBS5-c1
CBS5c5 segregants of mutant strain cao5 mt-
then obtained 1 842 meiotic segregants by cell mating random analysis and wild type segregants were not detected
the result confirmed that mutant genes cbn1 and cao was close linkage;50 segregants were obtained by cell mating tetrat analysis and wild type segregants were also not detected
the result further indicated that the mutant genes cbn1 and CAO have allelic characters;According to CAO sequence
were probes were designsed relating to 5′-end and 3′-end of CAO
DNA dot blot was carried out to use above two probes with 21 BAC clones between two molecular marker GBP1 and RB47 on chlamydomonas linkagegroupⅠ
positive spot was detected in hybridization of 33e2 BAC clone with both two probes
the result indicated the position of the CAO on the molecular map was on the 33e2 BAC clone which located between GBP1 and RB47.
J.-D.R ocha ix&S.M erchan t.T heM o lecu lar B io logy of Ch lorop lasts andM itochondria in Ch lam yd om onas[M].Boston,U.S.A:K luw er A cadem ic pub lishers,1998.
A yum i T anaka,H isash i Ito,R you ich iT anaka.Ch lorophy ll a oxygenase(CAO)is invo lved in ch lorophy ll b form ationfrom ch lorophy ll a[J].P lan t B io logy,1998,95,12719-12723.
U lrike O ster,R you ich i T anaka,A yum i T anaka.C lon ing and functiona l express ion of the gene encod ing the keyenzym e for ch lorophy ll b b iosyn thes is(CAO)from A rabid op sis tha liana[J].T he P lan t Journa l,2000,21,305-309.
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