Phyllostachys edulis, one of the most dominant bamboo species with the leptomorph rhizome system, has been asexually expanding its range into adjacent natural forest sites by shooting new culms. The resulting ecological problems include simplification of stand structure and decline in the species diversity of local flora. In this study, the genetic diversity of P. edulis for the entire distribution range from Japan to China was analyzed using 16 microsatellite markers. Among these, 12 loci were fixed by a single allele, whereas only two alleles were detected for each of the remaining 4 loci; all adult samples shared the same genotype at all loci including the four heterozygous loci. These observations indicate that all current samples from Japan and China comprise an identical clone. The clone is distributed over more than 2,800 km with an estimated biomass of approximately 6.6 × 10(11) kg, which is exceptionally large. Among seedlings from flowering events in 2005 and 2006, 20 different genets were generated by recombination through selfing of a single flowering genet. Predominance of a single clone in the wild and a diverse composition of genets among seedlings suggest that the intermittent flowering of P. edulis in the wild has produced a variety of clones through recombination. However, the resulting seedlings cannot compete with other tree species or adult P. edulis, and almost all adult P. edulis growing in Japan and China likely propagated through vegetative reproduction of a single clone by human transplantation, and subsequently expanded into adjacent forest sites by shooting young sprouts. The relatively small size of the flowering area and rapid culm reproduction has led to the stability of P. edulis communities. However, the low genetic diversity is an important consideration for the long-term management of this prevailing bamboo species.
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Unlabelled: Once considered rare in eukaryotes, polycistronic mRNA expression has been identified in kinetoplastids and, more recently, green algae, red algae, and certain fungi. This study provides comprehensive evidence supporting the existence of polycistronic mRNA expression in the apicomplexan parasite . Leveraging long-read RNA-seq data from different parasite strains and using multiple long-read technologies, we demonstrate the existence of defined polycistronic transcripts containing 2-4 protein encoding genes, several validated with RT-PCR.
View Article and Find Full Text PDFExpression and purification of recombinant proteins in is a bedrock technique in biochemistry and molecular biology. Expression optimization requires testing different combinations of solubility tags, affinity purification techniques, and site-specific proteases. This optimization is laborious and time consuming as these features are spread across different vector series and require different cloning strategies with varying efficiencies.
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Faculdade de Zootecnia e Engenharia de Alimentos - FZEA, Universidade de São Paulo - USP, Pirassununga, SP, Brasil.
Somatic cell nuclear transfer (SCNT), or cloning, is used to reprogram cells and generate genetically identical embryos and animals. However, the cloning process is inefficient, limiting its application to producing valuable animals. In swine, cloning is mainly utilized to produce genetically modified animals.
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Departments of Neurology, University of Michigan, Ann Arbor, MI 48109; Departments of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI 48109; Neurology Service, VA Ann Arbor Healthcare System, Department of Veterans Affairs, Ann Arbor, MI 48105. Electronic address:
Stereotyped mutations in NOTCH3 drive CADASIL, the leading inherited cause of stroke and vascular dementia. The vast majority of these mutations result in alterations in the number of cysteines in the gene product. However, non-cysteine altering pathogenic mutations have also been identified, making it challenging to discriminate pathogenic from benign NOTCH3 sequence variants.
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Research Center for Life Sciences Computing, Zhejiang Lab, Hangzhou 311100, China.
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