Brachiopod and mollusc biomineralisation is a conserved process that was lost in the phoronid-bryozoan stem lineage.

IF 4.1 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Evodevo Pub Date : 2022-09-19 DOI:10.1186/s13227-022-00202-8
Joel Vikberg Wernström, Ludwik Gąsiorowski, Andreas Hejnol
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引用次数: 4

Abstract

Background: Brachiopods and molluscs are lophotrochozoans with hard external shells which are often believed to have evolved convergently. While palaeontological data indicate that both groups are descended from biomineralising Cambrian ancestors, the closest relatives of brachiopods, phoronids and bryozoans, are mineralised to a much lower extent and are comparatively poorly represented in the Palaeozoic fossil record. Although brachiopod and mollusc shells are structurally analogous, genomic and proteomic evidence indicates that their formation involves a complement of conserved, orthologous genes. Here, we study a set of genes comprised of 3 homeodomain transcription factors, one signalling molecule and 6 structural proteins which are implicated in mollusc and brachiopod shell formation, search for their orthologs in transcriptomes or genomes of brachiopods, phoronids and bryozoans, and present expression patterns of 8 of the genes in postmetamorphic juveniles of the rhynchonelliform brachiopod T. transversa.

Results: Transcriptome and genome searches for the 10 target genes in the brachiopods Terebratalia transversa, Lingula anatina, Novocrania anomala, the bryozoans Bugula neritina and Membranipora membranacea, and the phoronids Phoronis australis and Phoronopsis harmeri resulted in the recovery of orthologs of the majority of the genes in all taxa. While the full complement of genes was present in all brachiopods with a single exception in L. anatina, a bloc of four genes could consistently not be retrieved from bryozoans and phoronids. The genes engrailed, distal-less, ferritin, perlucin, sp1 and sp2 were shown to be expressed in the biomineralising mantle margin of T. transversa juveniles.

Conclusions: The gene expression patterns we recovered indicate that while mineralised shells in brachiopods and molluscs are structurally analogous, their formation builds on a homologous process that involves a conserved complement of orthologous genes. Losses of some of the genes related to biomineralisation in bryozoans and phoronids indicate that loss of the capacity to form mineralised structures occurred already in the phoronid-bryozoan stem group and supports the idea that mineralised skeletons evolved secondarily in some of the bryozoan subclades.

腕足动物和软体动物的生物矿化是一个保守的过程,在栉虫-苔藓虫茎系中丢失了。
背景:腕足动物和软体动物是具有坚硬外壳的光栖动物,通常被认为是趋同进化的。虽然古生物学数据表明,这两个类群都是生物矿化的寒武纪祖先的后裔,但腕足类、栉虫类和苔藓虫的近亲矿化程度要低得多,在古生代化石记录中相对较少。尽管腕足动物和软体动物的壳在结构上是相似的,但基因组学和蛋白质组学证据表明,它们的形成涉及保守的同源基因的补充。本文研究了与软体动物和腕足动物壳形成有关的3个同源结构域转录因子、1个信号分子和6个结构蛋白组成的一组基因,在腕足动物、栉虫和苔藓虫的转录组或基因组中寻找了它们的同源物,并研究了其中8个基因在舌chonelliform腕足动物T. transversa后变态幼体中的表达模式。结果:对10个靶基因进行转录组和基因组搜索,在所有类群中恢复了大部分基因的同源性。其中,对横足类、鸭舌类、异常新妇足类、苔藓虫类、黑衣虫和膜孔虫进行了转录组和基因组搜索,获得了大部分基因的同源性。除了L. anatina有一个例外,所有腕足动物中都有完整的基因,而苔藓虫和栉虫中始终无法检索到四个基因。结果表明,在transversa幼体的生物矿化地幔边缘中表达了engrailed、远端less、ferritin、perlucin、sp1和sp2基因。结论:我们恢复的基因表达模式表明,虽然腕足类动物和软体动物的矿化壳在结构上是相似的,但它们的形成建立在一个涉及同源基因保守补体的同源过程上。苔藓虫和苔藓虫中与生物矿化有关的一些基因的缺失表明,形成矿化结构的能力的丧失已经发生在苔藓虫-苔藓虫茎群中,并支持矿化骨骼在某些苔藓虫亚分支中是次要进化的观点。
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来源期刊
Evodevo
Evodevo EVOLUTIONARY BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
7.50
自引率
0.00%
发文量
18
审稿时长
>12 weeks
期刊介绍: EvoDevo publishes articles on a broad range of topics associated with the translation of genotype to phenotype in a phylogenetic context. Understanding the history of life, the evolution of novelty and the generation of form, whether through embryogenesis, budding, or regeneration are amongst the greatest challenges in biology. We support the understanding of these processes through the many complementary approaches that characterize the field of evo-devo. The focus of the journal is on research that promotes understanding of the pattern and process of morphological evolution. All articles that fulfill this aim will be welcome, in particular: evolution of pattern; formation comparative gene function/expression; life history evolution; homology and character evolution; comparative genomics; phylogenetics and palaeontology
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