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绿色植物rbcL序列的系统发育分析。

Phylogenetic analysis of green plant rbcL sequences.

作者信息

Manhart J R

机构信息

Department of Biology, Texas A&M University, College Station 77843.

出版信息

Mol Phylogenet Evol. 1994 Jun;3(2):114-27. doi: 10.1006/mpev.1994.1014.

Abstract

DNA and derived amino acid sequences of the rbcL gene from selected photosynthetic bacteria, green algae, bryophytes, "fern allies," ferns, and seed plants were used to construct phylogenetic trees using parsimony algorithms. Internal support of clades was determined by the bootstrap and decay indices. External support was judged by comparison of trees with previous morphological and molecular cladograms. Some clades on all the trees are supported both internally and externally, but all of the trees are characterized by unsupported relationships of the bryophytes and fern allies. Trees produced by analyses of all three DNA positions have the highest levels of internal support, but many clades are still not supported externally or internally. Analyses using only the first and second positions of the DNA sequences and derived amino acid sequences produced trees with odd groupings and low levels of internal support for most of the clades. These results indicate that rbcL sequences may be too divergent to test phylogenetic relationships among major groups of green plants. Additional problems with constructing phylogenetic trees from rbcL sequences may be caused by RNA editing, pseudogenes, unequal rates of evolution, and inadequate taxon sampling. Whether RNA editing is a problem can be determined by sequencing amplified RNAs from selected taxa. If pseudogenes are suspected, purified chloroplast DNA should be used for amplification. It may be beneficial to include more taxa in subsequent analyses, but there are indications that historical extinctions will prevent adequate sampling of some groups, such as the bryophytes and fern allies.

摘要

利用简约算法,选用了光合细菌、绿藻、苔藓植物、“蕨类近缘植物”、蕨类植物和种子植物的rbcL基因的DNA及推导的氨基酸序列来构建系统发育树。分支的内部支持度由自展检验和衰减指数确定。通过将这些树与先前的形态学和分子分支图进行比较来判断外部支持度。所有树上的一些分支在内部和外部都得到了支持,但所有树的特征都是苔藓植物和蕨类近缘植物之间的关系缺乏支持。对所有三个DNA位置进行分析所产生的树具有最高水平的内部支持,但许多分支在外部或内部仍然没有得到支持。仅使用DNA序列的第一和第二位置以及推导的氨基酸序列进行分析,所产生的树具有奇怪的分组,并且大多数分支的内部支持度较低。这些结果表明,rbcL序列可能差异太大,无法检验绿色植物主要类群之间的系统发育关系。从rbcL序列构建系统发育树的其他问题可能由RNA编辑、假基因、不等进化速率和分类群抽样不足引起。RNA编辑是否是一个问题可以通过对选定分类群的扩增RNA进行测序来确定。如果怀疑存在假基因,则应使用纯化的叶绿体DNA进行扩增。在后续分析中纳入更多分类群可能是有益的,但有迹象表明,历史灭绝将阻碍对某些类群(如苔藓植物和蕨类近缘植物)进行充分抽样。

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