Genome-wide identification and transcriptional analysis of ammonium transporters in Saccharum

Genomics ◽  
2021 ◽  
Author(s):  
Zilin Wu ◽  
Xiaoning Gao ◽  
Nannan Zhang ◽  
Xiaomin Feng ◽  
Yonghong Huang ◽  
...  
2017 ◽  
Vol 40 (1 suppl 1) ◽  
pp. 346-359 ◽  
Author(s):  
Tiago Benedito dos Santos ◽  
Joni Esrom Lima ◽  
Mariane Silva Felicio ◽  
João Danillo Moura Soares ◽  
Douglas Silva Domingues

Author(s):  
Aimee N. Laporte ◽  
Neal M. Poulin ◽  
Alireza Lorzadeh ◽  
Xiu Qing Wang ◽  
Ryan Vander werff ◽  
...  

2005 ◽  
Vol 51 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Fredrik Karlsson ◽  
Ann-Christin Malmborg-Hager ◽  
Ann-Sofie Albrekt ◽  
Carl A.K Borrebaeck

To identify Escherichia coli genes potentially regulated by filamentous phage infection, we used oligonucleotide microarrays. Genome-wide comparison of phage M13-infected and uninfected E. coli, 2 and 20 min after infection, was performed. The analysis revealed altered transcription levels of 12 E. coli genes in response to phage infection, and the observed regulation of phage genes correlated with the known in vivo pattern of M13 mRNA species. Ten of the 12 host genes affected could be grouped into 3 different categories based on cellular function, suggesting a coordinated response. The significantly upregulated genes encode proteins involved in reactions of the energy-generating phosphotransferase system and transcription processing, which could be related to phage transcription. No genes belonging to any known E. coli stress response pathways were scored as upregulated. Furthermore, phage infection led to significant downregulation of transcripts of the bacterial genes gadA, gadB, hdeA, gadE, slp, and crl. These downregulated genes are normally part of the host stress response mechanisms that protect the bacterium during conditions of acid stress and stationary phase transition. The phage-infected cells demonstrated impaired function of the oxidative and the glutamate-dependent acid resistance systems. Thus, global transcriptional analysis and functional analysis revealed previously unknown host responses to filamentous phage infection.Key words: filamentous phage infection, global transcriptional analysis, AR, Escherichia coli.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Bei Wang ◽  
Qijiang Jin ◽  
Xiao Zhang ◽  
Neil S. Mattson ◽  
Huihui Ren ◽  
...  

2016 ◽  
Vol 90 (20) ◽  
pp. 9293-9304 ◽  
Author(s):  
Laura Mojardín ◽  
Margarita Salas

ABSTRACTThe study of phage-host relationships is essential to understanding the dynamic of microbial systems. Here, we analyze genome-wide interactions ofBacillus subtilisand its lytic phage ϕ29 during the early stage of infection. Simultaneous high-resolution analysis of virus and host transcriptomes by deep RNA sequencing allowed us to identify differentially expressed bacterial genes. Phage ϕ29 induces significant transcriptional changes in about 0.9% (38/4,242) and 1.8% (76/4,242) of the host protein-coding genes after 8 and 16 min of infection, respectively. Gene ontology enrichment analysis clustered upregulated genes into several functional categories, such as nucleic acid metabolism (including DNA replication) and protein metabolism (including translation). Surprisingly, most of the transcriptional repressed genes were involved in the utilization of specific carbon sources such as ribose and inositol, and many contained promoter binding-sites for the catabolite control protein A (CcpA). Another interesting finding is the presence of previously uncharacterized antisense transcripts complementary to the well-known phage ϕ29 messenger RNAs that adds an additional layer to the viral transcriptome complexity.IMPORTANCEThe specific virus-host interactions that allow phages to redirect cellular machineries and energy resources to support the viral progeny production are poorly understood. This study provides, for the first time, an insight into the genome-wide transcriptional response of the Gram-positive modelBacillus subtilisto phage ϕ29 infection.


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