Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Ribosome Profiling02:24

Ribosome Profiling

4.2K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
4.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Effects of Composition and Baking Temperature on the Properties of Low-Protein Cookies.

Food science & nutrition·2026
Same author

Bispecific antibody engineered extracellular vesicles redirect T cells to prevent postoperative epidural fibrosis.

Nature communications·2026
Same author

The phospholipid biosynthesis enzyme PlsB contains three distinct domains for membrane association, lysophosphatidic acid synthesis, and dimerization.

Protein science : a publication of the Protein Society·2026
Same author

Efficacy and Safety of a Topical Skincare Regimen with Tripeptide/Hexapeptide following Aesthetic Procedures: Analysis of Two Randomized, Split-Face Trials in Asian Subjects.

Dermatology and therapy·2026
Same author

Synergistic Effects of Alkali, Salt, and Thickness Reduction on the Preparation and Properties of Low-Protein Noodles.

Food science & nutrition·2026
Same author

An interpretable machine learning model integrating [<sup>18</sup>F]FDG PET/CT radiomics and clinical features for predicting perforation following chemotherapy in gastrointestinal lymphoma: a multicenter study.

European journal of nuclear medicine and molecular imaging·2026
Same journal

Spatiotemporal and hydrodynamic influences on microbial and exometabolite dynamics in coral reef and seagrass ecosystems.

The ISME journal·2026
Same journal

Photosynthesis-driven interactions in the phycosphere enhance bacterial extracellular superoxide production.

The ISME journal·2026
Same journal

Correction to: Keystone protist suppression triggers mesopredator release and biotic homogenization in complex soil microbial communities.

The ISME journal·2026
Same journal

Stoichiometric analysis of microbial communities links function, structure, and biomass carrying capacity.

The ISME journal·2026
Same journal

Isolation of Allocrenothrix methanica reveals distinct ecophysiologies of filamentous methanotrophs and adaptations to O2 limitation.

The ISME journal·2026
Same journal

Minimising decompression and warming during deep seawater collection increases abundance and activity of autochthonous bacteria and archaea.

The ISME journal·2026
See all related articles

Related Experiment Video

Updated: Mar 9, 2026

Transcriptome Analysis of Single Cells
07:27

Transcriptome Analysis of Single Cells

Published on: April 25, 2011

30.7K

Single-cell transcriptomics of small microbial eukaryotes: limitations and potential.

Zhenfeng Liu1, Sarah K Hu1, Victoria Campbell1

  • 1Department of Biological Sciences, University of Southern California, Los Angeles, CA, USA.

The ISME Journal
|January 7, 2017
PubMed
Summary
This summary is machine-generated.

Single-cell RNA sequencing shows lower transcript recovery in smaller microbial eukaryotes due to reduced mRNA levels. This highlights challenges for studying tiny protists using this powerful single-cell transcriptomics tool.

More Related Videos

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
10:12

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

Published on: January 10, 2019

19.2K
An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing
10:00

An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing

Published on: May 23, 2018

18.4K

Related Experiment Videos

Last Updated: Mar 9, 2026

Transcriptome Analysis of Single Cells
07:27

Transcriptome Analysis of Single Cells

Published on: April 25, 2011

30.7K
Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
10:12

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

Published on: January 10, 2019

19.2K
An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing
10:00

An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing

Published on: May 23, 2018

18.4K

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genomics

Background:

  • Single-cell transcriptomics offers potential for studying microbial eukaryotes.
  • Previous studies focused on larger microbial eukaryotes (>50 μm).
  • Microbial eukaryotes range significantly in size, down to 1 μm.

Purpose of the Study:

  • To assess the feasibility of single-cell RNA sequencing (scRNA-seq) for smaller microbial eukaryotes.
  • To identify limitations of scRNA-seq in small protists.
  • To understand gene expression variability in small microbial eukaryotes.

Main Methods:

  • Application of scRNA-seq to two small protists (8 and 15 μm).
  • Comparison of transcript recovery and gene expression randomness with bulk RNA-seq.
  • Analysis of mRNA copy numbers in small versus larger organisms.

Main Results:

  • scRNA-seq yielded lower transcript recovery rates in smaller protists.
  • Higher randomness in observed gene expression levels was noted for smaller cells.
  • Lower mRNA copy numbers in smaller organisms were identified as the primary cause.

Conclusions:

  • Current scRNA-seq methods face limitations for studying small microbial eukaryotes (<15 μm).
  • Reduced mRNA abundance significantly impacts transcript recovery and data reliability.
  • Further methodological advancements are needed to overcome these challenges for small organism transcriptomics.