Research suggests core nuclear pore elements shared by all eukaryotes
July 13, 2009(PhysOrg.com) -- For perhaps 1.8 billion years after life first emerged on Earth, a sort of evolutionary writer’s block stalled the development of organisms more complicated than single cells. Then, a burst of experimental creativity about 1.7 billion years ago brought the cell nucleus onto the scene, stashing the cell’s genetic material inside a protective inner membrane and setting the stage for the evolution of more sophisticated creatures from yeast, say, to plants and human beings. Now research shows that one of the most basic design principles of this new eukaryotic life-form — the gatekeeper to the cell nucleus known as the nuclear pore complex — is largely shared across the most distantly related eukaryotes. Its core components likely evolved once and for all and would be found in the nuclear pore complex of what is known as the last common eukaryotic ancestor.
The findings, by Rockefeller University researchers Brian T. Chait, Michael P. Rout and colleagues, add details to an unfolding picture of cellular evolution that shows a common architecture for the nuclear pore complex and the vehicles that evolved around the same time to transport cargoes between different parts of the cell, called coated vesicles. As early as 1980, Rockefeller professor Günter Blobel proposed that the internal membranes of cells — such as those encompassing the nucleus and vesicles — evolved from invaginations of the outer cell membrane. Rout and Chait suggested in 2004 that the nuclear pore complex and vesicle coats, which both contain α-solenoid and β-propeller protein folds, evolved from ancient molecules called protocoatomers that stabilized the membranes of these primordial internal structures.
“This work shows that the pore contains the signature of this ancient evolutionary event,” says Rout, head of the Laboratory of Cellular and Structural Biology. “Some evolutionary biologists have argued that the resemblance is only superficial. This paper shows that that is not true. The resemblance is not skin deep. Indeed, it goes all the way to the core.”
Published June 13 in Molecular & Cellular Proteomics, research performed by former graduate student Jeffrey A. DeGrasse, now at the United States Food and Drug Administration, picked apart the proteins that make up the nuclear pore complex of Trypanosoma brucei, a deadly, single-celled parasite responsible for African sleeping sickness. In the evolutionary tree of eukaryotic life, T. brucei is about as far removed from vertebrates like ourselves as possible, far more distant than commonly used model organisms such as yeast, fungi and plants. “The trypanosomes were at the wedding of the eukaryotes but were divorced the day after,” says Rout, quoting his University of Cambridge colleague Mark C. Field, who also worked on the research. The idea is that if the nuclear pore complex proteins of trypanosomes are the same as those in vertebrates, then they almost certainly are also in the hypothetical cell known as the last common eukaryotic ancestor. “They are defining features of eukaryotes, just as warm blood plus hair form a defining feature of mammals,” says Rout.
Prior research had led other scientists to question whether the nuclear pore complex proteins are in fact conserved because they had found that the amino acid sequences that make up the proteins are quite different among far-flung eukaryotic species. DeGrasse and colleagues, working with highly enriched samples of nuclear pore complexes from our distant parasitic relative, also found that the amino acid sequences are not well conserved, based on a Basic Local Alignment Search Tool analysis of mass spectroscopy data. But they took the analysis a step further. Working with Andrej Sali at the University of California, San Francisco, DeGrasse applied a variety of other bioinformatic tools including algorithms describing protein folds and sorted through an initial pool of 757 proteins to identify 30 candidate nuclear pore complex proteins, roughly the same number that makes up the nuclear pore complexes of yeast and vertebrates. The researchers were able to genomically tag 22 of the 30 proteins and establish that they are deeply related, or homologous, to known proteins in yeast and vertebrate nuclear pore complexes, specifically those proteins that form the core scaffold of the complex and other well-described structures.
“These proteins are conserved at the structural level, especially the pore coat and the core scaffold, but also the unfolded proteins that traffic molecules through the complex between the nucleus and cytoplasm,” says Chait, the Camille and Henry Dreyfus Professor and head of the Laboratory of Mass Spectrometry and Gaseous Ion Chemistry. “All of the main elements are there.”
More information: Molecular & Cellular Proteomics, June 13, 2009
Evidence for a shared nuclear pore complex architecture that is conserved from the last common eukaryotic ancestor
Jeffrey A. DeGrasse, Kelly N. DuBois, Damien Devos, T. Nicolai Siegel, Andrej Sali, Mark C. Field, Michael P. Rout and Brian T. Chait
-
Research identifies 3-D structure of key nuclear pore building block
Jun 07, 2009 |
not rated yet |
0
-
Researchers construct a device that mimics one of nature's key transport machines
Jan 06, 2009 |
not rated yet |
0
-
Multi-lab collaboration yields first detailed map of nuclear pore complex
Dec 03, 2007 |
not rated yet |
0
-
Structural study backs new model for the nuclear pore complex
Dec 24, 2008 |
not rated yet |
0
-
Building the nuclear pore piece by piece
Apr 16, 2007 |
not rated yet |
0
-
Engineers build first sub-10-nm carbon nanotube transistor
Feb 01, 2012 |
4.9 / 5 (32) |
30
-
Something old, something new: Evolution and the structural divergence of duplicate genes
Jan 31, 2012 |
4.6 / 5 (7) |
1
-
The hidden nanoworld of ice crystals: Revealing the dynamic behavior of quasi-liquid layers
Jan 30, 2012 |
5 / 5 (4) |
1
-
Stock market network reveals investor clustering
Jan 27, 2012 |
3.9 / 5 (23) |
8
-
Of microchemistry and molecules: Electronic microfluidic device synthesizes biocompatible probes
Jan 26, 2012 |
5 / 5 (2) |
0
-
How to determine zinc in a plant.
Feb 11, 2012
-
Stoichiometry
Feb 10, 2012
-
Boiling and melting point of impure substances
Feb 10, 2012
-
Safe nitrogen compound to decompose a 500 deg C in a furnace?
Feb 09, 2012
-
[ask]electron inside drinking water
Feb 08, 2012
-
How to avoid formation of Lithium Chromate ???
Feb 08, 2012
- More from Physics Forums - Chemistry
More news stories
Scientists discover molecular secrets of 2,000-year-old Chinese herbal remedy
For roughly two thousand years, Chinese herbalists have treated Malaria using a root extract, commonly known as Chang Shan, from a type of hydrangea that grows in Tibet and Nepal. More recent studies suggest that halofuginone, ...
1 hour ago |
5 / 5 (5) |
1
|
New method to examine batteries -- MRI from the inside
There is an ever-increasing need for advanced batteries for portable electronics, such as phones, cameras, and music players, but also to power electric vehicles and to facilitate the distribution and storage of energy derived ...
Chemistry / Analytical Chemistry
1 hour ago |
5 / 5 (1) |
0
|
Hydrogen from acidic water: Researchers develop potential low cost alternative to platinum for splitting water
A technique for creating a new molecule that structurally and chemically replicates the active part of the widely used industrial catalyst molybdenite has been developed by researchers with the Lawrence Berkeley ...
Feb 09, 2012 |
4.8 / 5 (16) |
21
|
Fool's gold may prove an unlikely alternative to overexploited catalytic materials
Catalytic materials, which lower the energy barriers for chemical reactions, are used in everything from the commercial production of chemicals to catalytic converters in car engines. However, with current catalytic materials ...
Feb 10, 2012 |
4.4 / 5 (8) |
8
|
Research provides octagonal window of opportunity for carbon capture
(PhysOrg.com) -- Filtering carbon dioxide, a greenhouse gas, from factory smokestacks is a necessary, but expensive part of many manufacturing processes. However, a collaborative research team from the National ...
Feb 08, 2012 |
5 / 5 (2) |
5
|
Lab study raises questions over nano-particle impact
Tests involving chickens have raised questions about the impact on health from engineered nano-particles, the ultra-fine grains commonly used in drugs and processed foods, scientists said on Sunday.
A mitosis mystery solved: How chromosomes align perfectly in a dividing cell
Although the process of mitotic cell division has been studied intensely for more than 50 years, Whitehead Institute researchers have only now solved the mystery of how cells correctly align their chromosomes during symmetric ...
Starve a virus, feed a cure? Findings show how some cells protect themselves against HIV
A protein that protects some of our immune cells from the most common and virulent form of HIV works by starving the virus of the molecular building blocks that it needs to replicate, according to research published online ...
Researchers find extensive RNA editing in human transcriptome
In a new study published online in Nature Biotechnology, researchers from BGI, the world's largest genomics organization, reported the evidence of extensive RNA editing in a human cell line by analysis of RNA-seq data, demons ...
The proteins ensuring genome protection
Researchers from the University of Geneva (UNIGE), Switzerland, have discovered the crucial role of two proteins in developing a cell 'anti-enzyme shield'. This protection system, which operates at the level of molecular ...
Google might launch Drive for cloud storage soon
(PhysOrg.com) -- Google's next big move, according to the Wall Street Journal, is a cloud storage service called Drive. Hardly first to the plate, Google is simply catching up to introducing its cloud reposi ...