Ribosome is an important machine that is inseparable from many life activities of organisms, such as cell proliferation and protein synthesis. The development of ribosomal transcriptomics has laid the foundation for further understanding of the protein synthesis process. Creative Biolabs is a leading ribosome analysis service provider. At Creative Biolabs, we focus on providing customized service to our global clients, we will help you promote your program to success.
Translation is an essential process in life. It outlines the process of converting genetic information in mRNA nucleotide sequences into proteins. Translation is carried out by the ribosome, which first recognizes the region of the mRNA that encodes the protein, then reads the codons one at a time, assembling a polypeptide whose amino acid sequence corresponds to the codon sequence. Therefore, to understand translation and its regulation, it is essential to determine the location and number of ribosomes on mRNA in vivo. Ribosomal profiling provides an opportunity to explore these locations as a novel strategy. Analysis of the ribosomal transcriptome primarily sequenced cDNA libraries derived from ribosome-covered mRNA short fragments, and ribosome profiling performed transcriptome-wide measurements of ribosome occupancy.
Fig.1 Schematic of genome-wide methods to study polysome-associated mRNAs. (Kapeli, 2012)
The transcriptome of the sample provides a more representative expression profile, reducing the search space by eliminating unexpressed gene products. Transcriptome also provides information about sequence variation, such as mutations and editing variations, which can aid in the detection of novel proteins. However, due to extensive translational regulation, the presence of transcripts does not correspond exactly to the presence of the corresponding protein. Recently, a new technique that attempts to address these limitations has been described: ribosome profiling. Breakthroughs in transcriptome analysis have been facilitated by advances in ribosome analysis.
We provide flexible analysis services which include but are not limited to:
A: Ribosomal transcriptome analysis involves sequencing cDNA libraries from ribosome-protected mRNA fragments to study the process of translation. This method helps in understanding how ribosomes select and translate mRNA into proteins, offering insights into protein synthesis and regulation.
A: With years of experience, an advanced technology platform, and a focus on cost-effectiveness and efficient project completion, Creative Biolabs provides a reliable choice for scientists seeking comprehensive ribosome analysis services, including post-analysis support. We offer a range of services including ribosome profiling, polysome profiling, ribosome complex profiling, and ribosome RNA sequencing services. These services are designed to support various research needs related to ribosome analysis.
A: Yes, Creative Biolabs focuses on providing customized ribosome analysis services to meet the specific needs of their global clients. They work closely with researchers to choose the optimal experimental procedures and techniques for each project.
GENOME RESEARCH
Authors: Peggy Janich, Alaaddin Bulak Arpat, Violeta Castelo-Szekely, et al.
Abstract:
Mammalian gene expression displays widespread circadian oscillations. Rhythmic transcription underlies the core clock mechanism, but it cannot explain numerous observations made at the level of protein rhythmicity. We have used ribosome profiling in mouse liver to measure the translation of mRNAs into protein around the clock and at high temporal and nucleotide resolution. We discovered, transcriptome-wide, extensive rhythms in ribosome occupancy and identified a core set of approximately 150 mRNAs subject to particularly robust daily changes in translation efficiency. Cycling proteins produced from nonoscillating transcripts revealed thus-far-unknown rhythmic regulation associated with specific pathways (notably in iron metabolism, through the rhythmic translation of transcripts containing iron responsive elements), and indicated feedback to the rhythmic transcriptome through novel rhythmic transcription factors. Moreover, estimates of relative levels of core clock protein biosynthesis that we deduced from the data explained known features of the circadian clock better than did mRNA expression alone. Finally, we identified uORF translation as a novel regulatory mechanism within the clock circuitry. Consistent with the occurrence of translated uORFs in several core clock transcripts, loss-of-function of Denr, a known regulator of reinitiation after uORF usage and of ribosome recycling, led to circadian period shortening in cells. In summary, our data offer a framework for understanding the dynamics of translational regulation, circadian gene expression, and metabolic control in a solid mammalian organ.
Transcriptome-wide analysis of transcript abundance and ribosome occupancy rhythms. (Janich, Peggy, et al., 2015)
The success of different experiments depends on appropriate experimental procedures and analytical methods. Scientists in Creative Biolabs will choose the optimal experimental procedures and techniques according to your project needs. Welcome to discuss your ribosome-related project with our experts. Please feel free to contact us for more details.
Reference
(USA)
(UK)
(Germany)