Department of Molecular Biology and Biochemistry, Simon Fraser University, 8888 University Drive, Burnaby, BCBC V5A 1S6, Canada.
Laboratoire de Physiologie Cellulaire et Végétale, CNRS, CEA, INRAE, Université Grenoble Alpes, IRIG, CEA Grenoble, 17 Avenue des Martyrs, 38000 Grenoble, France.
G3 (Bethesda). 2024 Oct 7;14(10). doi: 10.1093/g3journal/jkae181.
To thrive on melting alpine and polar snow, some Chlorophytes produce an abundance of astaxanthin, causing red blooms, often dominated by genus Sanguina. The red cells have not been cultured, but we recently grew a green biciliate conspecific with Sanguina aurantia from a sample of watermelon snow. This culture provided source material for Oxford Nanopore Technology and Illumina sequencing. Our assembly pipeline exemplifies the value of a hybrid long- and short-read approach for the complexities of working with a culture grown from a field sample. Using bioinformatic tools, we separated assembled contigs into 2 genomic pools based on a difference in GC content (57.5 and 55.1%). We present the data as 2 assemblies of S. aurantia variants but explore other possibilities. High-throughput chromatin conformation capture analysis (Hi-C sequencing) was used to scaffold the assemblies into a 96-Mb genome designated as "A" and a 102-Mb genome designated as "B." Both assemblies are highly contiguous: genome A consists of 38 scaffolds with an N50 of 5.4 Mb, while genome B has 50 scaffolds with an N50 of 6.4 Mb. RNA sequencing was used to improve gene annotation.
为了在融化的高山和极地雪中茁壮成长,一些绿藻产生大量虾青素,导致红色花朵的出现,这些花朵通常以 Sanguina 属为主。这些红色细胞尚未被培养,但我们最近从西瓜雪样本中培养出了一种与 Sanguina aurantia 同属的绿色双鞭毛生物。该培养物为牛津纳米孔技术和 Illumina 测序提供了材料来源。我们的组装管道展示了混合长读和短读方法对于处理从野外样本中培养的文化的复杂性的价值。使用生物信息学工具,我们根据 GC 含量的差异(57.5%和 55.1%)将组装的 contigs 分成 2 个基因组池。我们将数据呈现为 2 个 S. aurantia 变体的组装,但也探索了其他可能性。高通量染色质构象捕获分析(Hi-C 测序)用于将组装支架构建成一个 96-Mb 的基因组,称为“A”,以及一个 102-Mb 的基因组,称为“B”。这两个组装都具有高度连续性:基因组 A 由 38 个支架组成,N50 为 5.4 Mb,而基因组 B 有 50 个支架,N50 为 6.4 Mb。RNA 测序用于改进基因注释。