資金は、ゴードンとベティムーア財団の助成金と国立科学財団の助成金MCB - 0702125で提供されていました。

<ol>
	<li>Liang, P., Pardee, A. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Science. 257 (5072), 967-967 (1992).</li><li>Belasco, J. G., Belasco, J. G., Brawerman, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Control+of+messenger+RNA+stability.">Control of messenger RNA stability.</a> , 3-11 (1993).</li><li>Poretsky, R. S., Bano, N., Buchan, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> 71 (7), 4121-4121 (2005).</li><li>Gelder, R. N. V., von Zastrow, M. E., Yool, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Natl. Acad. Sci. USA. 87 (5), 1663-1663 (1990).</li><li>Margulies, M., Egholm, M., Altman, W. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Nature. 437 (7057), 376-376 (2005).</li><li>Frias-Lopez, J., Shi, Y., Tyson, G. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Natl. Acad. Sci. USA. 105 (10), 3805-3805 (2008).</li><li>Poretsky, R. S., Hewson, I., Sun, S., Allen, A. E., Zehr, J. P., Moran, M. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Environ Microbiol. 11 (6), 1358-1375 (2009).</li></ol>

天然の微生物群集による遺伝子発現の調査では、微生物の生態学的役割と機能を探求するための手段として近年一般的になっている。海洋微生物の検出、定量、および特性評価と組み合わせて使用​​される、遺伝子発現の解析は、自然の微生物群集に機能するように系統発生をリンクするために使用することができます。機能的な遺伝子発現を標的とするための多くの技術は、特定のプロ?...

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		<div>
		<table border="1">
		<thead>
		<tr>
		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
		</tr>
		</thead>
		<tbody>
		
<tr>
<td>PowerSoil Bead Tubes</td>
<td>kit</td>
<td>MoBio</td>
<td>12866-25-PBT</td>
<td>&nbsp;</td>
<tr>
<td>RNeasy Mini Kit</td>
<td>kit</td>
<td>QIAGEN</td>
<td>74104</td>
<td>&nbsp;</td>
<tr>
<td>TURBO DNA-free</td>
<td>kit</td>
<td>Ambion</td>
<td>AM1907</td>
<td>&nbsp;</td>
<tr>
<td>mRNA-ONLY Prokaryotic mRNA Isolation Kit</td>
<td>kit</td>
<td>Epicentre</td>
<td>MOP51010/MOP51024</td>
<td>&nbsp;</td>
<tr>
<td>MICROBExpress Bacterial mRNA Enrichment Kit</td>
<td>kit</td>
<td>Ambion</td>
<td>AM1905</td>
<td>&nbsp;</td>
<tr>
<td>MICROBEnrich kit</td>
<td>kit</td>
<td>Ambion</td>
<td>AM1901</td>
<td>&nbsp;</td>
<tr>
<td>MessageAmp II-Bacteria RNA Amplification Kit</td>
<td>kit</td>
<td>Ambion</td>
<td>AM1790</td>
<td>&nbsp;</td>
<tr>
<td>Universal RiboClone cDNA Synthesis System</td>
<td>kit</td>
<td>Promega</td>
<td>C4360</td>
<td>&nbsp;</td>
<tr>
<td>Wizard DNA Clean-Up System</td>
<td>kit</td>
<td>Promega</td>
<td>A7280</td>
<td>&nbsp;</td>		</tbody>
		</table>
		</div>

analyzing gene expression from marine microbial communities using environmental transcriptomics

コミュニティが表現されるかもしれないものの遺伝子の事前の知識がなくてもメタゲノム、環境トランスクリプト（metatranscriptomics）を取得し、配列の微生物集団からの環境のmRNAに似ています。したがって、コミュニティの遺伝子発現に最も公平な視点を提供<em&gt;その場で</em&gt;。原核生物のmRNAは、一般に真核生物のメッセージの分離は比較的簡単なようにポリ（A）テールが不足しているため、環境トランスクリプトミクスのプロトコルは、技術的に困難です。<sup&gt; 1</sup&gt;とするためのmRNAの比較的短い半減期の<sup&gt; 2</sup&gt;。さらに、mRNAがあまり豊富なトータルRNAの抽出物中のrRNAsよりも、こうしてrRNAの背景には、多くの場合、mRNAの信号を圧倒する。しかし、これらの困難のいくつかを克服するための手法が最近開発されている。逆転写と環境mRNAを増幅するためのランダムプライマーを用いてクローンライブラリを作成することにより、環境のトランスクリプトームを分析するための手順は、最近記述されていた二つの異なる自然環境では正常終了しましたが、結果はcDNA合成を開始するために使用されるランダムプライマーの選択によってバイアスされた<sup&gt; 3</sup&gt;。 mRNAの線形増幅の進歩により、増幅の段階でランダムプライマーの必要性を未然に防ぐ、それが可能なサンプルの収集と処理時間を減少し、それによってRNAの分解を最小限に少なく、出発物質を使用すること<sup&gt; 4</sup&gt;。<em&gt;試験管内で</em&gt;増幅mRNAの転写の方法は、mRNAをpolyadenylatingと転写産物の3末端にT7プロモーターを組み込んだ伴う。増幅RNA（aRNAを）パイロシーケンシングによって、ランダムヘキサマーを用いて本鎖cDNAをdouble型に変換されると直接配列決定することができます<sup&gt; 5</sup&gt;。駅ALOHAにおけるこのメソッドの最初の使用は、微生物群集の遺伝子発現を特徴付けるために、その有用性を実証<sup&gt; 6</sup&gt;。

Watch this Scientific Journal Video about Analyzing Gene Expression from Marine Microbial Communities using Environmental Transcriptomics at JoVE.com

Analyzing Gene Expression from Marine Microbial Communities using Environmental Transcriptomics

私たちは、環境のmRNAからcDNAを生成するための方法を提示する。一般的に、トータルRNAは、最初の環境から収集され、rRNAを選択的に除去され、mRNAが選択的に増幅され、濃縮mRNAのプールから合成したcDNAは、配列決定される。回収された配列は、発現遺伝子を識別するために、標準的なバイオインフォマティクス技術を用いて注釈を付けることができます。

環境トランスクリプトミクスを使って海洋微生物群集からの遺伝子発現の分析

Analogous to metagenomics, environmental transcriptomics (metatranscriptomics) retrieves and sequences environmental mRNAs from a microbial assemblage ...

analyzing-gene-expression-from-marine-microbial-communities-using

Research

JoVE Journal

Biology

12.4K ビュー.  University of Georgia (UGA). 私たちは、環境のmRNAからcDNAを生成するための方法を提示する。一般的に、トータルRNAは、最初の環境から収集され、rRNAを選択的に除去され、mRNAが選択的に増幅され、濃縮mRNAのプールから合成したcDNAは、配列決定される。回収された配列は、発現遺伝子を識別するために、標準的なバイオインフォマティクス技術を用いて注釈を付けることができます?...

ビデオ: Analyzing Gene Expression from Marine Microbial Communities using Environmental Transcriptomics

Microbial Communities in Nature and Laboratory - Interview

自然と実験室での微生物群集 - インタビュー

生物学

Biology of Microbial Communities  - Interview

微生物群集の生物学 - インタビュー

Bacterial Gene Expression Analysis Using Microarrays

マイクロアレイを用いた細菌の遺伝子発現解析

The Preparation of Primary Hematopoietic Cell Cultures From Murine Bone Marrow for Electroporation

It is becoming increasingly apparent that electroporation is the most effective way to introduce plasmid DNA or siRNA into primary cells. The Gene Pulser MXcell  electroporation system and Gene Pulser  electroporation buffer were specifically developed to transfect nucleic acids into mammalian cells and difficult-to-transfect cells, such as primary and stem cells.This video demonstrates how to establish primary hematopoietic cell cultures from murine bone marrow, and then prepare them for electroporation in the MXcell system. We begin by isolating femur and tibia. Bone marrow from both femur and tibia are then harvested and cultures are established. Cultured bone marrow cells are then transfected and analyzed.

This procedure describes how to establish primary hematopoietic cell cultures from murine bone marrow and is followed by transfection using the Gene Pulser MXCell electroporation system.

エレクトロポレーションのためのマウス骨髄からの一次造血細胞培養の準備

It is becoming increasingly apparent that electroporation is the most effective way to introduce plasmid DNA or siRNA into primary cells. The Gene Pulser ...

Using the Gene Pulser MXcell Electroporation System to Transfect Primary Cells with High Efficiency

It is becoming increasingly apparent that electroporation is the most effective way to introduce plasmid DNA or siRNA into primary cells. The Gene Pulser MXcell electroporation system and Gene Pulser electroporation buffer (Bio-Rad) were specifically developed to easily transfect nucleic acids into mammalian cells and difficult-to-transfect cells, such as primary and stem cells. We will demonstrate how to perform a simple experiment to quickly identify the best electroporation conditions. We will demonstrate how to run several samples through a range of electroporation conditions so that an experiment can be conducted at the same time as optimization is performed. We will also show how optimal conditions identified using 96-well electroporation plates can be used with standard electroporation cuvettes, facilitating the switch from electroporation plates to electroporation cuvettes while maintaining the same electroporation efficiency. In the video, we will also discuss some of the key factors that can lead to the success or failure of electroporation experiments.

This procedure shows how to use the Gene Pulser MXcell electroporation system to rapidly and easily identify the best electroporation conditions for mouse embryonic fibroblasts (MEFs) or other primary cells. Considerations for troubleshooting are also discussed in the associated video.

高効率で初代培養細胞をトランスフェクトするためにジーンパルサーMXcellのエレクトロポレーションシステムの使用

Using an Automated Cell Counter to Simplify Gene Expression Studies: siRNA Knockdown of IL-4 Dependent Gene Expression in Namalwa Cells

The use of siRNA mediated gene knockdown is continuing to be an important tool in studies of gene expression.  siRNA studies are being conducted not only to study the effects of downregulating single genes, but also to interrogate signaling pathways and other complex interaction networks.  These pathway analyses require both the use of relevant cellular models and methods that cause less perturbation to the cellular physiology.  Electroporation is increasingly being used as an effective way to introduce siRNA and other nucleic acids into difficult to transfect cell lines and primary cells without altering the signaling pathway under investigation. There are multiple critical steps to a successful siRNA experiment, and there are ways to simplify the work while improving the data quality at several experimental stages.  To help you get started with your siRNA mediated gene knockdown project, we will demonstrate how to perform a pathway study complete from collecting and counting the cells prior to electroporation through post transfection real-time PCR gene expression analysis.  The following study investigates the role of the transcriptional activator STAT6 in IL-4 dependent gene expression of CCL17 in a Burkitt lymphoma cell line (Namalwa).  The techniques demonstrated are useful for a wide range of siRNA-based experiments on both adherent and suspension cells.  We will also show how to streamline cell counting with the TC10 automated cell counter, how to electroporate multiple samples simultaneously using the MXcell electroporation system, and how to simultaneously assess RNA quality and quantity with the Experion automated electrophoresis system.

This procedure describes a quick and easy workflow to introduce siRNA into difficult to transfect cell lines and follow gene expression by real-time PCR. Use of an automated cell counter, multi-well electroporation plate, and automated electrophoresis station provide quick and reliable results without the need for expensive robotic handling.

ナマルバ細胞におけるIL - 4依存性遺伝子発現のsiRNAのノックダウン：遺伝子発現研究を簡素化する自動化セルカウンターの使い方

The use of siRNA mediated gene knockdown is continuing to be an important tool in studies of gene expression.  siRNA studies are being conducted not only ...

In vitro Reconstitution of the Active T. castaneum Telomerase

Efforts to isolate the catalytic subunit of telomerase, TERT, in sufficient quantities for structural studies, have been met with limited success for more than a decade. Here, we present methods for the isolation of the recombinant Tribolium castaneum TERT (TcTERT) and the reconstitution of the active T. castaneum telomerase ribonucleoprotein (RNP) complex in vitro.
Telomerase is a specialized reverse transcriptase1 that adds short DNA repeats, called telomeres, to the 3' end of linear chromosomes2 that serve to protect them from end-to-end fusion and degradation. Following DNA replication, a short segment is lost at the end of the chromosome3 and without telomerase, cells continue dividing until eventually reaching their Hayflick Limit4. Additionally, telomerase is dormant in most somatic cells5 in adults, but is active in cancer cells6 where it promotes cell immortality7.
The minimal telomerase enzyme consists of two core components: the protein subunit (TERT), which comprises the catalytic subunit of the enzyme and an integral RNA component (TER), which contains the template TERT uses to synthesize telomeres8,9. Prior to 2008, only structures for individual telomerase domains had been solved10,11. A major breakthrough in this field came from the determination of the crystal structure of the active12, catalytic subunit of T. castaneum telomerase, TcTERT1.
Here, we present methods for producing large quantities of the active, soluble TcTERT for structural and biochemical studies, and the reconstitution of the telomerase RNP complex in vitro for telomerase activity assays. An overview of the experimental methods used is shown in Figure 1.

In vitro Reconstitution of the Active T. castaneum Telomerase

Efforts to isolate the catalytic subunit of telomerase, TERT, in sufficient quantities for structural studies, have been met with limited success for more than a decade. Here, we present methods for the isolation of the recombinant Tribolium castaneum TERT (TcTERT) and the reconstitution of the active T. castaneum telomerase ribonucleoprotein (RNP) complex in vitro.

アクティブT.の試験管内再構成でcastaneumのテロメラーゼ

Efforts to isolate the catalytic subunit of telomerase, TERT, in sufficient quantities for structural studies, have been met with limited success for more ...

Extraction of High Molecular Weight DNA from Microbial Mats

Successful and accurate analysis and interpretation of metagenomic data is dependent upon the efficient extraction of high-quality, high molecular weight (HMW) community DNA. However, environmental mat samples often pose difficulties to obtaining large concentrations of high-quality, HMW DNA. Hypersaline microbial mats contain high amounts of extracellular polymeric substances (EPS)1 and salts that may inhibit downstream applications of extracted DNA. Direct and harsh methods are often used in DNA extraction from refractory samples. These methods are typically used because the EPS in mats, an adhesive matrix, binds DNA2,3 during direct lysis. As a result of harsher extraction methods, DNA becomes fragmented into small sizes4,5,6.
The DNA thus becomes inappropriate for large-insert vector cloning. In order to circumvent these limitations, we report an improved methodology to extract HMW DNA of good quality and quantity from hypersaline microbial mats. We employed an indirect method involving the separation of microbial cells from the background mat matrix through blending and differential centrifugation. A combination of mechanical and chemical procedures was used to extract and purify DNA from the extracted microbial cells. Our protocol yields approximately 2 &mu;g of HMW DNA (35-50 kb) per gram of mat sample, with an A260/280 ratio of 1.6. Furthermore, amplification of 16S rRNA genes7 suggests that the protocol is able to minimize or eliminate any inhibitory effects of contaminants. Our results provide an appropriate methodology for the extraction of HMW DNA from microbial mats for functional metagenomic studies and may be applicable to other environmental samples from which DNA extraction is challenging.

We provide an improved protocol for extracting high molecular weight DNA from hypersaline microbial mats. Microbial cells are separated from the mat matrix prior to DNA extraction and purification. This enhances the concentrations, quality, and size of the DNA. The protocol may be used for other refractory samples.

バイオマットから高分子量DNAの抽出

Successful and accurate analysis and interpretation of metagenomic data is dependent upon the efficient extraction  of high-quality, high molecular weight ...

Concentration of Metabolites from Low-density Planktonic Communities for Environmental Metabolomics using Nuclear Magnetic Resonance Spectroscopy

Environmental metabolomics is an emerging field that is promoting new understanding in how organisms respond to and interact with the environment and each other at the biochemical level1. Nuclear magnetic resonance (NMR) spectroscopy is one of several technologies, including gas chromatography&#x2013;mass spectrometry (GC-MS), with considerable promise for such studies. Advantages of NMR are that it is suitable for untargeted analyses, provides structural information and spectra can be queried in quantitative and statistical manners against recently available databases of individual metabolite spectra2,3. In addition, NMR spectral data can be combined with data from other omics levels (e.g. transcriptomics, genomics) to provide a more comprehensive understanding of the physiological responses of taxa to each other and the environment4,5,6. However, NMR is less sensitive than other metabolomic techniques, making it difficult to apply to natural microbial systems where sample populations can be low-density and metabolite concentrations low compared to metabolites from well-defined and readily extractable sources such as whole tissues, biofluids or cell-cultures. Consequently, the few direct environmental metabolomic studies of microbes performed to date have been limited to culture-based or easily defined high-density ecosystems such as host-symbiont systems, constructed co-cultures or manipulations of the gut environment where stable isotope labeling can be additionally used to enhance NMR signals7,8,9,10,11,12. Methods that facilitate the concentration and collection of environmental metabolites at concentrations suitable for NMR are lacking. Since recent attention has been given to the environmental metabolomics of organisms within the aquatic environment, where much of the energy and material flow is mediated by the planktonic community13,14, we have developed a method for the concentration and extraction of whole-community metabolites from planktonic microbial systems by filtration. Commercially available hydrophilic poly-1,1-difluoroethene (PVDF) filters are specially treated to completely remove extractables, which can otherwise appear as contaminants in subsequent analyses. These treated filters are then used to filter environmental or experimental samples of interest. Filters containing the wet sample material are lyophilized and aqueous-soluble metabolites are extracted directly for conventional NMR spectroscopy using a standardized potassium phosphate extraction buffer2. Data derived from these methods can be analyzed statistically to identify meaningful patterns, or integrated with other omics levels for comprehensive understanding of community and ecosystem function.

A method for metabolite extraction from microbial planktonic communities is presented. Whole community sampling is achieved by filtration onto specially prepared filters. After lyophilization, aqueous-soluble metabolites are extracted. This approach allows for application of environmental metabolomics to trans-omics investigations of natural or experimental microbial communities.

核磁気共鳴分光法を用いた環境メタボロミクスのための低密度プランクトンコミュニティからの代謝物の濃度

Environmental metabolomics is an emerging field that is promoting new understanding in how organisms respond to and interact with the environment and each ...

Analysis of Global RNA Synthesis at the Single Cell Level following Hypoxia

Hypoxia or lowering of the oxygen availability is involved in many physiological and pathological processes. At the molecular level, cells initiate a particular transcriptional program in order to mount an appropriate and coordinated cellular response. The cell possesses several oxygen sensor enzymes that require molecular oxygen as cofactor for their activity. These range from prolyl-hydroxylases to histone demethylases. The majority of studies analyzing cellular responses to hypoxia are based on cellular populations and average studies, and as such single cell analysis of hypoxic cells are seldom performed. Here we describe a method of analysis of global RNA synthesis at the single cell level in hypoxia by using Click-iT RNA imaging kits in an oxygen controlled workstation, followed by microscopy analysis and quantification.&nbsp; Using cancer cells exposed to hypoxia for different lengths of time, RNA is labeled and measured in each cell. This analysis allows the visualization of temporal and cell-to-cell changes in global RNA synthesis following hypoxic stress.

We describe a technique for analysis of global RNA synthesis in hypoxia using imaging. Click-chemistry labeling of RNA has not previously been performed under hypoxia and allows visualization of global RNA changes at the single cell level. This approach complements the existing averaged RNA techniques, allowing direct visualization of cell-to-cell changes in global RNA synthesis.

低酸素症後単一細胞レベルでのグローバルのRNA合成の分析

Hypoxia or lowering of the oxygen availability is involved in many physiological and pathological processes. At the molecular level, cells initiate a ...