Saccharina japonica is a major kelp species of brown algae with the highest production among aquaculture seaweeds and holds important ecological and economic value. Despite advancements in domestication, a high-quality chromosome-level genome assembly is needed to assist its genetic improvement. Previous genome assemblies of S. japonica were either on a draft-level or highly fragmented. Here, we generated a high-quality chromosome-level genome for the female sporophyte using PacBio sequencing and Hi-C. The genome is 516.11 Mb, with contig N50 length of 491.30 Kb and scaffold N50 length of 16.24 Mb, anchored into 32 pseudo-chromosomes. Repetitive elements constituted 45.07% of the genome, and 17,739 protein-coding genes were predicted, of which 82% were functionally annotated. This genome provides a crucial resource for biotechnological advances in S. japonica breeding and offers insights into the ecology and evolution of brown algae.

Wild-type sporophytes of Saccharina japonica have been recurrently observed on the infrastructures of kelp farming rafts in China’s northern production region (Liaoning and Shandong provinces). However, there are few detailed reports delineating their origin, genetic attributes and affiliations with farmed populations. Using microsatellite molecular analyses, we furnish a comparative analysis of the populations sampled from these rafts at one of the historical kelp farming regions Rongcheng city (Shandong province), both before and after the “2021–2022 kelp farming disaster”, in conjunction with two field populations from nearby intertidal zones where natural populations prevail. The results show that the wild kelp populations on the kelp farming rafts in 2023 had originated from the wild populations dwelling in intertidal zones several kilometers away, rather than from the artificially cultivated kelp cultivars.

Background/Objectives: Desiccation profoundly influences the distribution and abundance of intertidal seaweeds, necessitating robust molecular adaptations. Sargassum muticum is a brown seaweed inhabiting intertidal rocky substrates. During low tides, this species undergoes periodic aerial exposure. Such environmental conditions necessitate robust physiological mechanisms to mitigate desiccation stress. Yet, the molecular basis of this adaptation remains poorly understood. Methods: To investigate desiccation-responsive genes and elucidate the underlying mechanisms of adaptation, we exposed S. muticum to 6 h of controlled desiccation stress in sterilized ceramic trays, simulating natural tidal conditions, and performed comparative transcriptome analysis using RNA-seq on the Illumina NovaSeq 6000 platform. Results: High-quality sequencing identified 66,192 unigenes, with 1990 differentially expressed genes (1399 upregulated and 591 downregulated). These differentially expressed genes (DEGs) were categorized into regulatory genes—including mitogen-activated protein kinase (MAPK), calmodulin, elongation factor, and serine/threonine-protein kinase—and functional genes, such as heat shock protein family members (HSP20, HSP40, and HSP70), tubulin (TUBA and TUBB), and endoplasmic reticulum homeostasis-related genes (protein disulfide-isomerase A6, calreticulin, and calnexin). Gene Ontology (GO) enrichment highlighted upregulated DEGs in metabolic processes like glutathione metabolism, critical for oxidative stress mitigation, while downregulated genes were linked to transport functions, such as ammonium transport, suggesting reduced nutrient uptake during dehydration. KEGG pathway analysis revealed significant enrichment in “protein processing in endoplasmic reticulum” and “MAPK signaling pathway-plant”, implicating endoplasmic reticulum stress response and conserved signaling cascades in desiccation adaptation. Validation via qRT-PCR confirmed consistent expression trends for key genes, reinforcing the reliability of transcriptomic data. Conclusions: These findings suggest that S. muticum undergoes extensive biological adjustments to mitigate desiccation stress, highlighting candidate pathways for future investigations into recovery and tolerance mechanisms.