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首页> 外文期刊>PLoS One >Analysis of small and large subunit rDNA introns from several ectomycorrhizal fungi species
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Analysis of small and large subunit rDNA introns from several ectomycorrhizal fungi species

机译:几种突出菌毒性真菌物种中小型亚基RDNA内含子分析

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The small (18S) and large (28S) nuclear ribosomal DNA (rDNA) introns have been researched and sequenced in a variety of ectomycorrhizal fungal taxa in this study, it is found that both 18S and 28S rDNA would contain introns and display some degree variation in size, nucleotide sequences and insertion positions within the same fungi species ( Meliniomyces ). Under investigations among the tested isolates, 18S rDNA has four sites for intron insertions, 28S rDNA has two sites for intron insertions. Both 18S and 28S rDNA introns among the tested isolates belong to group I introns with a set of secondary structure elements designated P1-P10 helics and loops. We found a 12 nt nucleotide sequences TACCACAGGGAT at site 2 in the 3’-end of 28S rDNA, site 2 introns just insert the upstream or the downstream of the12 nt nucleotide sequences. Afters sequence analysis of all 18S and 28S rDNA introns from tested isolates, three high conserved regions around 30 nt nucleotides (conserved 1, conserved 2, conserved 3) and identical nucleotides can be found. Conserved 1, conserved 2 and conserved 3 regions have high GC content, GC percentage is almost more than 60%. From our results, it seems that the more convenient host sites, intron sequences and secondary structures, or isolates for 18S and 28S rDNA intron insertion and deletion, the more popular they are. No matter 18S rDNA introns or 18S rDNA introns among tested isolates, complementary base pairing at the splicing sites in P1-IGS-P10 tertiary helix around 5’-end introns and exons were weak.
机译:在本研究中已经研究和大(28岁)和大(28秒)核核糖体DNA(RDNA)内含子在该研究中的各种外霉菌真菌分类群中进行测序,发现18S和28S rDNA含有内含子并显示一些程度的变化在相同的真菌物种(Meliniomyces)的大小,核苷酸序列和插入位置。在测试分离株中的调查中,18秒具有内含子插入的四个位点,28s RDNA具有用于内含子插入的两个位点。在测试的隔离物中的18秒和28s RDNA内含子属于I组内含子,其中一组二次结构元件指定为P1-P10螺旋和环。我们在28S rDNA的3'-末端发现了12nt核苷酸序列Taccacagggat,位点2内含物仅插入12 nT核苷酸序列的上游或下游。从测试分离株的所有18s和28s rDNA内含子的偏移序列分析,可以发现三个高保守区域(保守1,保守2,保守3)和相同的核苷酸。保守1,保守2和保守3个区域具有高GC含量,GC百分比几乎超过60%。从我们的结果中,似乎更方便的主站点,内含子序列和二级结构,或分离为18秒和28秒内含子插入和删除,它们越受欢迎。无论18s RDNA内含子或18秒内含子内含子,在测试分离物中,P1-IGS-P10第三六个螺旋中的剪接位点处的互补碱基配对差弱。

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