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

Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes02:16

Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes

The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
The Anatomy of Chloroplasts01:08

The Anatomy of Chloroplasts

Green algae and plants, including green stems and unripe fruit, harbor specialized organelles called chloroplasts to carry out photosynthesis. They coordinate both stages of photosynthesis — the light-dependent reactions and the light-independent reactions. The light-dependent reactions use sunlight to release oxygen and produce chemical energy in the form of ATP and NADPH, and the light-independent reactions capture CO2 and use ATP and NADPH to produce sugar.
Structure of Chloroplasts
A...
Eukaryotic Evolution01:24

Eukaryotic Evolution

The endosymbiont theory is the most widely accepted theory of eukaryotic evolution; however, its progression is still somewhat debated. According to the nucleus-first hypothesis, the ancestral prokaryote first evolved a membrane to enclose DNA and form the nucleus. Conversely, the mitochondria-first hypothesis suggests that the nucleus was formed after endosymbiosis of mitochondria.
Contrary to the endosymbiont theory, the eukaryote-first hypothesis proposes that the simpler prokaryotic and...
Export of Mitochondrial and Chloroplast Genes02:19

Export of Mitochondrial and Chloroplast Genes

A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred irrespective...
Microbial Phylogeny01:28

Microbial Phylogeny

Understanding the evolutionary relationships among microorganisms is fundamental to microbial ecology and taxonomy. Phylogenetic trees are essential tools for inferring these relationships, relying primarily on comparative analyses of molecular sequences such as DNA, RNA, or proteins. In microbial studies, these trees typically depict the evolutionary paths of diverse bacterial and archaeal species by mapping genetic differences accumulated over time.Phylogenetic trees are composed of tips,...
Overview of Protists01:27

Overview of Protists

Protists are diverse eukaryotic microorganisms that lack the specialized tissues of plants and animals and the chitinous cell walls of fungi. Their early divergence within Eukarya resulted in structural, functional, and ecological diversity. They are classified into supergroups such as Archaeplastida, Excavata, Amoebozoa, Rhizaria, Alveolata, and Stramenopiles, determined through genetic analysis and structural similarities.Structural and Functional AdaptationsProtists have various adaptations...

You might also read

Related Articles

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

Sort by
Same author

Scythicorhinus vekuai gen. nov. et comb. nov. (Mammalia, Rhinocerotidae) from the Pliocene of Georgia and its implications for the early evolution of Coelodonta and Stephanorhinus.

Scientific reports·2026
Same author

Phylogeographic and demographic responses of Eurasian moose to climate change since the Late Pleistocene.

Heredity·2026
Same author

Temporal and gene-specific dynamics of codon usage evolution in SARS-CoV-2 genomes.

BMC genomics·2026
Same author

Elongator complex differentially regulates transcription and translation in the hypocotyl and cotyledons during early light-dependent Arabidopsis development.

Plant & cell physiology·2026
Same author

The evolutionary history of Rhinocerotidae: phylogenetic insights and climate influences.

Cladistics : the international journal of the Willi Hennig Society·2025
Same author

The Role of Mutations, Addition of Amino Acids, and Exchange of Genetic Information in the Coevolution of Primitive Coding Systems.

International journal of molecular sciences·2025

Related Experiment Video

Updated: Jun 19, 2026

Visualizing Stromule Frequency with Fluorescence Microscopy
08:27

Visualizing Stromule Frequency with Fluorescence Microscopy

Published on: November 23, 2016

Early steps in plastid evolution: current ideas and controversies.

Andrzej Bodył1, Paweł Mackiewicz, John W Stiller

  • 1Department of Biodiversity and Evolutionary Taxonomy, Zoological Institute, University of Wrocław, Wrocław, Poland. bodyl@biol.uni.wroc.pl

Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|October 23, 2009
PubMed
Summary

The endomembrane (EM) system is not the primary pathway for nuclear-encoded protein import into plant plastids. Instead, ancestral protein translocon (Toc and Tic) evolution likely preceded EM trafficking for plastid development.

More Related Videos

Preparation of Chloroplast Sub-compartments from Arabidopsis for the Analysis of Protein Localization by Immunoblotting or Proteomics
10:28

Preparation of Chloroplast Sub-compartments from Arabidopsis for the Analysis of Protein Localization by Immunoblotting or Proteomics

Published on: October 19, 2018

Plastoglobule Lipid Droplet Isolation from Plant Leaf Tissue and Cyanobacteria
10:35

Plastoglobule Lipid Droplet Isolation from Plant Leaf Tissue and Cyanobacteria

Published on: October 6, 2022

Related Experiment Videos

Last Updated: Jun 19, 2026

Visualizing Stromule Frequency with Fluorescence Microscopy
08:27

Visualizing Stromule Frequency with Fluorescence Microscopy

Published on: November 23, 2016

Preparation of Chloroplast Sub-compartments from Arabidopsis for the Analysis of Protein Localization by Immunoblotting or Proteomics
10:28

Preparation of Chloroplast Sub-compartments from Arabidopsis for the Analysis of Protein Localization by Immunoblotting or Proteomics

Published on: October 19, 2018

Plastoglobule Lipid Droplet Isolation from Plant Leaf Tissue and Cyanobacteria
10:35

Plastoglobule Lipid Droplet Isolation from Plant Leaf Tissue and Cyanobacteria

Published on: October 6, 2022

Area of Science:

  • Plant biology
  • Cellular and molecular biology
  • Evolutionary biology

Background:

  • Nuclear-encoded proteins are imported into higher plant plastids.
  • The endomembrane (EM) system was proposed as an early mechanism for protein import.
  • Modern plastid protein import relies on Toc and Tic translocons.

Purpose of the Study:

  • To re-evaluate the role of the endomembrane (EM) system in early plastid evolution.
  • To compare the evolutionary origins of EM trafficking versus Toc/Tic translocon pathways.
  • To assess the parsimony of different hypotheses regarding protein import evolution.

Main Methods:

  • Comparative analysis of protein transport mechanisms.
  • Review of empirical and theoretical data on plastid import pathways.
  • Evolutionary hypothesis testing.

Main Results:

  • The endomembrane (EM) system's role in plastid protein import is less significant than initially suggested.
  • Early plastid evolution likely involved simpler, ancestral forms of Toc and Tic translocons for post-translational import.
  • EM trafficking likely evolved later to accommodate specific functions like glycosylation.

Conclusions:

  • The evolution of Toc and Tic translocons predates the widespread use of the EM system for plastid protein import.
  • EM trafficking is a later adaptation, not the primary ancestral mechanism for plastid protein import.
  • The hypothesis of early Toc/Tic evolution is supported by available data and the limited EM-based transport in modern plastids.