Probiotics effectively prevent and improve metabolic diseases
such as diabetes by regulating the intestinal microenvironment
and gut microbiota. However, the effects of probiotics
in gestational diabetes mellitus are not clear. Here, we
showed that probiotic supplements significantly improved
fasting blood glucose in a gestational diabetes mellitus rat
model. To further understand the mechanisms of probiotics
in gestational diabetes mellitus, the gut microbiota were analyzed
via 16S rRNA sequencing. We found that compared
with the normal pregnant group, the gestational diabetes mellitus
rats had decreased diversity of gut microbiota. Moreover,
probiotic supplementation restored the diversity of the
gut microbiota in gestational diabetes mellitus rats, and the
gut microbiota structure tended to be similar to that of normal
pregnant rats. In particular, compared with gestational
diabetes mellitus rats, the abundance of Firmicutes and Actinobacteria
was higher after probiotic supplementation. Furthermore,
activating carbohydrate metabolism and membrane
transport pathways may be involved in the potential mechanisms
by which probiotic supplements alleviate gestational
diabetes mellitus. Overall, our results suggested that probiotic
supplementation might be a novel approach to restore the gut
microbiota of gestational diabetes mellitus rats and provided
an experimental evidence for the use of probiotic supplements
to treat gestational diabetes melitus.
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Multiple transcriptional regulators play important roles in
the coordination of developmental processes, including asexual
and sexual development, and secondary metabolism in the
filamentous fungus Aspergillus nidulans. In the present study,
we characterized a novel putative C2H2-type transcription
factor (TF), RocA, in relation to development and secondary
metabolism. Deletion of rocA increased conidiation and caused
defective sexual development. In contrast, the overexpression
of rocA exerted opposite effects on both phenotypes. Additionally,
nullifying rocA resulted in enhanced brlA expression
and reduced nsdC expression, whereas its overexpression
exerted the opposite effects. These results suggest that RocA
functions as a negative regulator of asexual development by
repressing the expression of brlA encoding a key asexual development
activator, but as a positive regulator of sexual development
by enhancing the expression of nsdC encoding a
pivotal sexual development activator. Deletion of rocA increased
the production of sterigmatocystin (ST), as well as the
expression of its biosynthetic genes, aflR and stcU. Additionally,
the expression of the biosynthetic genes for penicillin
(PN), ipnA and acvA, and for terrequinone (TQ), tdiB and
tdiE, was increased by rocA deletion. Thus, it appears that
RocA functions as a negative transcriptional modulator of the
secondary metabolic genes involved in ST, PN, and TQ biosynthesis.
Taken together, we propose that RocA is a novel
transcriptional regulator that may act either positively or negatively
at multiple target genes necessary for asexual and
sexual development and secondary metabolism.
Identification of a Novel Pleiotropic Transcriptional Regulator Involved in Sporulation and Secondary Metabolism Production in Chaetomium globosum Shanshan Zhao, Kai Zhang, Congyu Lin, Ming Cheng, Jinzhu Song, Xin Ru, Zhengran Wang, Wan Wang, Qian Yang International Journal of Molecular Sciences.2022; 23(23): 14849. CrossRef
System-wide studies of a given molecular type are referred
to as “omics.” These include genomics, proteomics, and metabolomics,
among others. Recent biotechnological advances
allow for high-throughput measurement of cellular components,
and thus it becomes possible to take a snapshot of all
molecules inside cells, a form of omics study. Advances in
computational modeling methods also make it possible to
predict cellular mechanisms from the snapshots. These technologies
have opened an era of computation-based biology.
Component snapshots allow the discovery of gene-phenotype
relationships in diseases, microorganisms in the human
body, etc. Computational models allow us to predict new outcomes,
which are useful in strain design in metabolic engineering
and drug discovery from protein-ligand interactions.
However, as the quantity of data increases or the model
becomes complicated, the process becomes less accessible
to biologists. In this special issue, six protocol articles
are presented as user guides in the field of computational
biology.
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Automation of Drug Discovery through Cutting-edge In-silico Research in
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Regulator of RNase E activity modulates the pathogenicity of Salmonella Typhimurium Jaejin Lee, Eunkyoung Shin, Ji-Hyun Yeom, Jaeyoung Park, Sunwoo Kim, Minho Lee, Kangseok Lee Microbial Pathogenesis.2022; 165: 105460. CrossRef
Transcript-specific selective translation by specialized ribosomes bearing genome-encoded heterogeneous rRNAs in V. vulnificus CMCP6 Younkyung Choi, Minju Joo, Wooseok Song, Minho Lee, Hana Hyeon, Hyun-Lee Kim, Ji-Hyun Yeom, Kangseok Lee, Eunkyoung Shin Journal of Microbiology.2022; 60(12): 1162. CrossRef
Omics-based microbiome analysis in microbial ecology: from sequences to information Jang-Cheon Cho Journal of Microbiology.2021; 59(3): 229. CrossRef
Trans-acting regulators of ribonuclease activity Jaejin Lee, Minho Lee, Kangseok Lee Journal of Microbiology.2021; 59(4): 341. CrossRef
Regulator of ribonuclease activity modulates the pathogenicity of Vibrio vulnificus Jaejin Lee, Eunkyoung Shin, Jaeyeong Park, Minho Lee, Kangseok Lee Journal of Microbiology.2021; 59(12): 1133. CrossRef
Gene expression changes in response to diverse environmental
stimuli to regulate numerous cellular functions. Genes are expressed
into their functional products with the help of messenger
RNA (mRNA). Thus, measuring levels of mRNA in
cells is important to understand cellular functions. With advances
in next-generation sequencing (NGS), the abundance
of cellular mRNA has been elucidated via transcriptome sequencing.
However, several studies have found a discrepancy
between mRNA abundance and protein levels induced by
translational regulation, including different rates of ribosome
entry and translational pausing. As such, the levels of mRNA
are not necessarily a direct representation of the protein levels
found in a cell. To determine a more precise way to measure
protein expression in cells, the analysis of the levels of mRNA
associated with ribosomes is being adopted. With an aid of
NGS techniques, a single nucleotide resolution footprint of
the ribosome was determined using a method known as Ribo-
Seq or ribosome profiling. This method allows for the highthroughput
measurement of translation in vivo, which was
further analyzed to determine the protein synthesis rate, translational
pausing, and cellular responses toward a variety of
environmental changes. Here, we describe a simple analysis
pipeline for Ribo-Seq in bacteria, so-called simple translatome
analysis tool for Ribo-Seq (STATR). STATR can be
used to carry out the primary processing of Ribo-Seq data,
subsequently allowing for multiple levels of translatome study,
from experimental validation to in-depth analyses. A command-
by-command explanation is provided here to allow a
broad spectrum of biologists to easily reproduce the analysis.
Citations
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Translation in Bacillus subtilis is spatially and temporally coordinated during sporulation Olga Iwańska, Przemysław Latoch, Natalia Kopik, Mariia Kovalenko, Małgorzata Lichocka, Remigiusz Serwa, Agata L. Starosta Nature Communications.2024;[Epub] CrossRef
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Omics-based microbiome analysis in microbial ecology: from sequences to information Jang-Cheon Cho Journal of Microbiology.2021; 59(3): 229. CrossRef
HRIBO: high-throughput analysis of bacterial ribosome profiling data Rick Gelhausen, Sarah L Svensson, Kathrin Froschauer, Florian Heyl, Lydia Hadjeras, Cynthia M Sharma, Florian Eggenhofer, Rolf Backofen, Valencia Alfonso Bioinformatics.2021; 37(14): 2061. CrossRef
User guides for biologists to learn computational methods Dokyun Na Journal of Microbiology.2020; 58(3): 173. CrossRef