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轮藻纲绿藻星芒鼓藻属和双星藻属的完整叶绿体DNA序列表明,在双星藻目的进化过程中,叶绿体基因组发生了广泛的变化。

The complete chloroplast DNA sequences of the charophycean green algae Staurastrum and Zygnema reveal that the chloroplast genome underwent extensive changes during the evolution of the Zygnematales.

作者信息

Turmel Monique, Otis Christian, Lemieux Claude

机构信息

Département de Biochimie et de Microbiologie, Université Laval, Québec, Québec, G1K 7P4, Canada.

出版信息

BMC Biol. 2005 Oct 20;3:22. doi: 10.1186/1741-7007-3-22.

DOI:10.1186/1741-7007-3-22
PMID:16236178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1277820/
Abstract

BACKGROUND

The Streptophyta comprise all land plants and six monophyletic groups of charophycean green algae. Phylogenetic analyses of four genes from three cellular compartments support the following branching order for these algal lineages: Mesostigmatales, Chlorokybales, Klebsormidiales, Zygnematales, Coleochaetales and Charales, with the last lineage being sister to land plants. Comparative analyses of the Mesostigma viride (Mesostigmatales) and land plant chloroplast genome sequences revealed that this genome experienced many gene losses, intron insertions and gene rearrangements during the evolution of charophyceans. On the other hand, the chloroplast genome of Chaetosphaeridium globosum (Coleochaetales) is highly similar to its land plant counterparts in terms of gene content, intron composition and gene order, indicating that most of the features characteristic of land plant chloroplast DNA (cpDNA) were acquired from charophycean green algae. To gain further insight into when the highly conservative pattern displayed by land plant cpDNAs originated in the Streptophyta, we have determined the cpDNA sequences of the distantly related zygnematalean algae Staurastrum punctulatum and Zygnema circumcarinatum.

RESULTS

The 157,089 bp Staurastrum and 165,372 bp Zygnema cpDNAs encode 121 and 125 genes, respectively. Although both cpDNAs lack an rRNA-encoding inverted repeat (IR), they are substantially larger than Chaetosphaeridium and land plant cpDNAs. This increased size is explained by the expansion of intergenic spacers and introns. The Staurastrum and Zygnema genomes differ extensively from one another and from their streptophyte counterparts at the level of gene order, with the Staurastrum genome more closely resembling its land plant counterparts than does Zygnema cpDNA. Many intergenic regions in Zygnema cpDNA harbor tandem repeats. The introns in both Staurastrum (8 introns) and Zygnema (13 introns) cpDNAs represent subsets of those found in land plant cpDNAs. They represent 16 distinct insertion sites, only five of which are shared by the two zygnematalean genomes. Three of these insertions sites have not been identified in Chaetosphaeridium cpDNA.

CONCLUSION

The chloroplast genome experienced substantial changes in overall structure, gene order, and intron content during the evolution of the Zygnematales. Most of the features considered earlier as typical of land plant cpDNAs probably originated before the emergence of the Zygnematales and Coleochaetales.

摘要

背景

链形植物包括所有陆地植物以及绿藻门轮藻纲的六个单系类群。对来自三个细胞区室的四个基因进行系统发育分析,支持了这些藻类谱系的以下分支顺序:中带藻目、绿囊藻目、鞘毛藻目、双星藻目、鞘藻目和轮藻目,其中最后一个谱系是陆地植物的姐妹群。对中带藻(中带藻目)和陆地植物叶绿体基因组序列的比较分析表明,在轮藻纲的进化过程中,该基因组经历了许多基因丢失、内含子插入和基因重排。另一方面,球囊藻(鞘藻目)的叶绿体基因组在基因含量、内含子组成和基因顺序方面与陆地植物的对应基因组高度相似,这表明陆地植物叶绿体DNA(cpDNA)的大多数特征是从绿藻门轮藻纲获得的。为了进一步深入了解陆地植物cpDNA所呈现的高度保守模式在链形植物中何时起源,我们测定了远缘双星藻目藻类斑点角星鼓藻和环绕双星藻的cpDNA序列。

结果

斑点角星鼓藻的157,089 bp cpDNA和环绕双星藻的165,372 bp cpDNA分别编码121个和125个基因。虽然这两个cpDNA都缺乏编码rRNA的反向重复序列(IR),但它们比球囊藻和陆地植物的cpDNA大得多。这种增大的大小是由基因间隔区和内含子的扩展来解释的。斑点角星鼓藻和环绕双星藻的基因组在基因顺序水平上彼此之间以及与它们的链形植物对应基因组有很大差异,斑点角星鼓藻的基因组比环绕双星藻的cpDNA更类似于陆地植物的对应基因组。环绕双星藻cpDNA中的许多基因间隔区含有串联重复序列。斑点角星鼓藻(8个内含子)和环绕双星藻(13个内含子)cpDNA中的内含子代表了陆地植物cpDNA中发现的内含子的子集。它们代表16个不同的插入位点,其中只有5个是这两个双星藻目基因组共有的。这些插入位点中有3个在球囊藻cpDNA中未被鉴定到。

结论

在双星藻目的进化过程中,叶绿体基因组在整体结构、基因顺序和内含子含量方面经历了重大变化。大多数先前被认为是陆地植物cpDNA典型特征的特征可能在双星藻目和鞘藻目出现之前就已经起源了。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/c5d1f7330733/1741-7007-3-22-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/46b225e649ad/1741-7007-3-22-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/87671b19ee9b/1741-7007-3-22-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/6441d0c8a511/1741-7007-3-22-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/a602c2212775/1741-7007-3-22-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/c5d1f7330733/1741-7007-3-22-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/46b225e649ad/1741-7007-3-22-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/87671b19ee9b/1741-7007-3-22-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/6441d0c8a511/1741-7007-3-22-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/a602c2212775/1741-7007-3-22-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3392/1277820/c5d1f7330733/1741-7007-3-22-5.jpg

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