scholarly journals Characterization of Methanosarcina mazei JL01 Isolated from Holocene Arctic Permafrost and Study of the Archaeon Cooperation with Bacterium Sphaerochaeta associata GLS2T

Proceedings ◽  
2020 ◽  
Vol 66 (1) ◽  
pp. 4
Author(s):  
Viktoriia Oshurkova ◽  
Olga Troshina ◽  
Vladimir Trubitsyn ◽  
Yana Ryzhmanova ◽  
Olga Bochkareva ◽  
...  
Keyword(s):  
Carbon Sources ◽  
Close Relation ◽  
Russian Arctic ◽  
Gram Stain ◽  
Optimum Conditions ◽  
Protein Coding ◽  
Methanosarcina Mazei ◽  
Protein Coding Genes

A mesophilic methanogenic culture, designated JL01, was isolated from Holocene permafrost in the Russian Arctic. After long-term extensive cultivation at 15 °C, it turned out to be a tied binary culture of archaeal (JL01) and bacterial (Sphaerochaeta associata GLS2) strains. Strain JL01 was a strict anaerobe and grew on methanol, acetate, and methylamines as energy and carbon sources. Cells were irregular coccoid, non-motile, non-spore-forming, and Gram-stain-positive. Optimum conditions for growth were 24–28 °C, pH 6.8–7.3, and 0.075–0.1 M NaCl. Phylogenetic tree reconstructions based on 16S rRNA and concatenated alignment of broadly conserved protein-coding genes revealed 16S rRNA’s close relation to Methanosarcina mazei S-6T (similarity 99.5%). The comparison of whole genomic sequences (ANI) of the isolate and the type strain of M. mazei was 98.5%, which is higher than the values recommended for new species. Thus, strain JL01 (=VKM B-2370 = JCM 31898) represents the first M. mazei isolated from permanently subzero Arctic sediments. The long-term co-cultivation of JL01 with S. associata GLS2T showed the methane production without any additional carbon and energy sources. Genome analysis of S. associata GLS2T revealed putative genes involved in methanochondroitin catabolism.

scholarly journals Identification and characterization of cis-regulatory elements for photoreceptor type-specific transcription in zebrafish

2019 ◽  
Author(s):  
Wei Fang ◽  
Yi Wen ◽  
Xiangyun Wei
Keyword(s):  
Core Promoter ◽  
Regulatory Elements ◽  
Specific Gene ◽  
Protein Coding ◽  
Core Promoters ◽  
Protein Coding Genes ◽  
The Core ◽  
Cell Type Specific ◽  
Identification And Characterization

AbstractTissue-specific or cell type-specific transcription of protein-coding genes is controlled by both trans-regulatory elements (TREs) and cis-regulatory elements (CREs). However, it is challenging to identify TREs and CREs, which are unknown for most genes. Here, we describe a protocol for identifying two types of transcription-activating CREs—core promoters and enhancers—of zebrafish photoreceptor type-specific genes. This protocol is composed of three phases: bioinformatic prediction, experimental validation, and characterization of the CREs. To better illustrate the principles and logic of this protocol, we exemplify it with the discovery of the core promoter and enhancer of the mpp5b apical polarity gene (also known as ponli), whose red, green, and blue (RGB) cone-specific transcription requires its enhancer, a member of the rainbow enhancer family. While exemplified with an RGB cone-specific gene, this protocol is general and can be used to identify the core promoters and enhancers of other protein-coding genes.

scholarly journals Computer programs for the characterization of protein coding genes

1984 ◽  
Vol 12 (1Part1) ◽  
pp. 281-285 ◽  
Author(s):  
G. Pierno ◽  
N. Barni ◽  
M. Candurro ◽  
M. Cipollaro ◽  
A. Franzè ◽  
...  
Keyword(s):  
Computer Programs ◽  
Protein Coding ◽  
Protein Coding Genes

scholarly journals Characterization of the mitochondrial genome of Analcellicampa xanthosoma gen. et sp. nov. (Hymenoptera: Tenthredinidae)

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e6866 ◽  
Author(s):  
Gengyun Niu ◽  
Yaoyao Zhang ◽  
Zhenyi Li ◽  
Meicai Wei
Keyword(s):  
Mitochondrial Genome ◽  
New Genus ◽  
Complete Mitochondrial Genome ◽  
Sister Group ◽  
Mitochondrial Genomes ◽  
Protein Coding ◽  
Protein Coding Genes ◽  
A New Species ◽  
High Support

A new genus with a new species of the tribe Hoplocampini of Hoplocampinae was described from China: Analcellicampa xanthosoma Wei & Niu, gen. et sp. nov. Hoplocampa danfengensis G. Xiao 1994 was designated as the type species of the new genus. The characters of Analcellicampa danfengensis (G. Xiao) comb. nov. were briefly discussed. A key to the tribes and known genera of Hoplocampinae was provided. The nearly complete mitochondrial genome of A. xanthosoma was characterized as having a length of 15,512 bp and containing 37 genes (22 tRNAs, 13 protein-coding genes (PCGs), and 2 rRNAs). The gene order of this new specimen was the same as that in the inferred insect ancestral mitochondrial genome. All PCGs were initiated by ATN codons and ended with TAA or T stop codons. All tRNAs had a typical cloverleaf secondary structure, except for trnS1. Remarkably, the helices H991 of rrnS and H47 of rrnL were redundant, while helix H563 of rrnL was highly conserved. A phylogeny based on previously reported symphytan mitochondrial genomes showed that A. xanthosoma is a sister group to Monocellicampa pruni, with high support values. We suggest that A. xanthosoma and M. pruni belong to the tribe Hoplocampini of Hoplocampinae.

scholarly journals Fact or fiction: updates on how protein-coding genes might emerge de novo from previously non-coding DNA

F1000Research ◽  
2017 ◽  
Vol 6 ◽  
pp. 57 ◽  
Author(s):  
Jonathan F Schmitz ◽  
Erich Bornberg-Bauer
Keyword(s):  
De Novo ◽  
Protein Structures ◽  
Divergence Times ◽  
Protein Coding ◽  
Future Studies ◽  
Functional Studies ◽  
Protein Coding Genes ◽  
Open Questions ◽  
Bona Fide

Over the last few years, there has been an increasing amount of evidence for the de novo emergence of protein-coding genes, i.e. out of non-coding DNA. Here, we review the current literature and summarize the state of the field. We focus specifically on open questions and challenges in the study of de novo protein-coding genes such as the identification and verification of de novo-emerged genes. The greatest obstacle to date is the lack of high-quality genomic data with very short divergence times which could help precisely pin down the location of origin of a de novo gene. We conclude that, while there is plenty of evidence from a genetics perspective, there is a lack of functional studies of bona fide de novo genes and almost no knowledge about protein structures and how they come about during the emergence of de novo protein-coding genes. We suggest that future studies should concentrate on the functional and structural characterization of de novo protein-coding genes as well as the detailed study of the emergence of functional de novo protein-coding genes.

scholarly journals Sequencing and Characterization of Mitochondrial Protein-Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Tasleem Akhtar ◽  
Ghazanfar Ali ◽  
Nuzhat Shafi ◽  
Wasim Akhtar ◽  
Abdul Hameed Khan ◽  
...  
Keyword(s):  
Amino Acids ◽  
Nadh Dehydrogenase ◽  
Mitochondrial Protein ◽  
Coi Gene ◽  
Nadh Dehydrogenase Subunit ◽  
Protein Coding ◽  
Protein Coding Genes ◽  
High Bootstrap ◽  
Atpase 6

The present study was conducted to get more information about the genome and locate the taxonomic position of Schizothorax niger in Schizothoracinae through mitochondrial 13 protein-coding genes (PCGs). These PCGs for S. niger were found to be 11409 bps in length ranging from 165 (ATPase 8) to 1824 bps (NADH dehydrogenase subunit 5) and encode 3801 amino acids. In these PCGs, 4 genes overlap on the similar strands, while one shown on the opposite one: ATPase 6+8 and NADH dehydrogenase subunit 4+4L overlap by 7 nucleotides. Similarly, ND5-ND6 overlap by 4 nucleotides, while ATP6 and COIII overlap by 1 nucleotide. Similarly, four commonly used amino acids in S. niger were Leu (15.6 %), Ile (10.12 %), Thr (8.12 %), and Ala (8.7 %). The results presented that COII, COIII, NDI, ND4L, and Cytb had substantial amino acid conservation as compared to the COI gene. Through phylogenetic analysis, it was observed that S. niger is closely linked with S. progastus, S. labiatus, S. plagiostomus, and S. nepalensis with high bootstrap values. The present study provided more genomic data to know the diversity of the mitochondrial genome and its molecular evolution in Schizothoracinae.

scholarly journals Genetic characterization of cysteine-rich type-b avenin-like protein coding genes in common wheat

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
X. Y. Chen ◽  
X. Y. Cao ◽  
Y. J. Zhang ◽  
S. Islam ◽  
J. J. Zhang ◽  
...  
Keyword(s):  
Common Wheat ◽  
Genetic Characterization ◽  
Type B ◽  
Protein Coding ◽  
Protein Coding Genes

scholarly journals An integrative atlas of chicken long non-coding genes and their annotations across 25 tissues

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Frédéric Jehl ◽  
Kévin Muret ◽  
Maria Bernard ◽  
Morgane Boutin ◽  
Laetitia Lagoutte ◽  
...  
Keyword(s):  
Transcription Factors ◽  
Biological Processes ◽  
Rna Seq ◽  
Protein Coding ◽  
Tissue Specific ◽  
Protein Coding Genes ◽  
Intergenic Regions ◽  
Immune Tissues ◽  
Non Coding Rnas

AbstractLong non-coding RNAs (LNC) regulate numerous biological processes. In contrast to human, the identification of LNC in farm species, like chicken, is still lacunar. We propose a catalogue of 52,075 chicken genes enriched in LNC (http://www.fragencode.org/), built from the Ensembl reference extended using novel LNC modelled here from 364 RNA-seq and LNC from four public databases. The Ensembl reference grew from 4,643 to 30,084 LNC, of which 59% and 41% with expression ≥ 0.5 and ≥ 1 TPM respectively. Characterization of these LNC relatively to the closest protein coding genes (PCG) revealed that 79% of LNC are in intergenic regions, as in other species. Expression analysis across 25 tissues revealed an enrichment of co-expressed LNC:PCG pairs, suggesting co-regulation and/or co-function. As expected LNC were more tissue-specific than PCG (25% vs. 10%). Similarly to human, 16% of chicken LNC hosted one or more miRNA. We highlighted a new chicken LNC, hosting miR155, conserved in human, highly expressed in immune tissues like miR155, and correlated with immunity-related PCG in both species. Among LNC:PCG pairs tissue-specific in the same tissue, we revealed an enrichment of divergent pairs with the PCG coding transcription factors, as for example LHX5, HXD3 and TBX4, in both human and chicken.

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