Showing posts with label cell. Show all posts
Showing posts with label cell. Show all posts

The Evolution Of Cooperation

Biology concepts – biological timeline, serial endosymbiosis, endocystosis, evolution


Taxonomy, the placing of species in different
groups based on their characteristics, changes
everyday – literally everyday – organisms are
placed in different groups and groups are created
and eliminated. That better be a temporary tattoo!
If we look at the 3.5 billion year history of life on Earth, we see that out planet was lifeless for almost a quarter of its span, and animals have been around just a short blip of time, a mere 760 million years. Often, it seems that the big numbers to get in the way of understanding the time line as a whole.

If we treat the entire history of earth as one year, we might get a clearer picture. Earth coalesces from space dust on January 1st, but it isn’t until March 22nd that we find the first evidence of life. These most primitive fossils are of the prokaryotes called Archaea (Greek for “ancient”). Not long after this, maybe a week or so, the eubacteria and Archaea separate from one another.

Then we have to wait until August 7th to find a big change; the first eukaryotic organisms are seen. These represent a fundamental change in the organisms, having nuclei and membrane bound organelles. It's amazing that we must travel 3/4 through our one year time line before we see a cell that looks somewhat like ours!


Here is one of the Namibia sponge fossils recently
discovered in Africa. It represents the oldest animal
in the fossil record. Just how that was recognized as a
fossil is beyond me – I think I have six of those in my
garden!
Later in the year, around October 30th at noon, we see the first animals. Fossils of Namibia sponges in Africa were first reported in February of 2012. This fossils are 100 million years older than the previously oldest animal remains, so our new data means that animals have been around for an additional week in our time line of a year.

Insects appear about Nov. 26th, while mammals first show up around Dec. 8th. The dinosaurs became extinct sometime in the afternoon of Dec. 26th, so they had very little time to play with their Christmas presents. Homo sapiens (us) didn’t appear on the doorstep looking for holiday cheer until 11:40 pm on New Years Eve, Dec. 31st!

Our time line analogy shows us that prokaryotes are the wise old ancestors; we aren’t even old enough to be rebellious teenagers, although we still think we know everything. The key question is: how did we progress to analogy-makers from single celled Archaea? If we put together several of the topics we have been discussing in the past three weeks, we may come up with an interesting step in the process. Our clues include:

1) Microcompartments exist in bacteria, like organelles, and they also exist in eukaryotic cells, especially in nucleus' function. This links eukaryotes to prokaryotes.

2) Sometimes cells will engulf objects, parts of other cells, or other cells. Depending on the size of the particle or cell, we may call this endocytosis or phagocytosis, and is similar to how we saw keratinocytes take up melanosomes.

3) Three eukaryotic organelles, the nucleus, the mitochondria, and the chloroplast have double membranes, and they each have their own DNA.

4) There are two different types of prokaryotes, archaea and bacteria.

Bacterial microcompartments give prokaryotes some compartmentalization in order to carry out necessary chemical reactions. Eukaryotes also have some prokaryotic microcompartment remnants, like the nuclear vault complex. This shows crossover between prokaryotes and eukaryotes, and gives us clues about eukaryotic origins. In fact, the currently accepted theory about the evolution of organelles - the very thing that makes cells eukaryotic - has to do with both types of prokaryotes - archaea and bacteria.


There are three types of endocytosis (with exceptions).
Endocystosis of large objects and cells is called phagocytosis.
Internalization of very small molecules and fluid is called
pinocytosis. Other molecules of various sizes have specific
receptors that recognize them on the cell surface. They are
brought in by receptor-mediated endocytosis. Notice that no
matter what method is used, the internalized particle ends up
surrounded by part of the cell membrane.
The key to their interrelationship has to do with endocytosis (endo = into, cyto = cell). Most prokaryotic and eukaryotic cells eat other cells; they do it all the time – it is how heterotrophic organisms (those that can't make their own carbohydrates, ie. non-plants) gain their nutrients. We do it too, just on a larger scale; we eat millions of cells at a time; often these millions of cells can take the shape of a steak or a carrot.

When a cell, protein, other molecule is engulfed by another cell, it is wrapped in a portion of the aggressor cell’s membrane. The naked molecule is now contained in a vesicle, a membrane bound sac, like the melanosome. If the endocytosed material is an entire cell, something that has its own membrane, then it ends up with two membranes, just like the mitochondrion, chloroplast, and nucleus.

Most often, when one prokaryote phagocytoses another, the story is over….gulp, yum, digest. But scientists believe that long ago (sometime in the first week of August in our time line) an endocytosed cell did not go gentle into that good night. Instead, it took up residence in the cell that ate it. In this rare case, it turned out that both cells gained from the situation.

The endocytosed cell was protected from other predators and had a ready supply of nutrients from the parent cell. The captured cell made lots of ATP, but it didn’t need much because it was being supplied with everything it needed; it didn't need to make energy to move or hunt or escape. Most of its ATP production went unused. Perhaps it moved this excess ATP out into the parent cell. So the parent cell gained a source of ATP production. This was mutualism, a type of symbiosis in which both parties benefit.


Clownfish clean the sea anemone and keep it
parasite free. The poisonous anemone provides
a safe environment for the clown fish; no
unwanted house guests! This is a good example of
mutualistic symbiosis. Bet you didn’t know you
learned things from Finding Nemo.
Imagine if the same thing happened with a cyanobacterium, a cell that could perform photosynthesis. The same sort of symbiosis might be set up, with the endocystosed cell providing carbohydrates and the parent cell providing protection.

Now imagine that these captured cells, the photosynthesizer and the ATP maker, replicated themselves inside their parent cells just as they would if they were outside, living on their own. They could easily do this since they still retained their own DNA and cell division mechanisms.

This is in fact what scientists believe happened. The endocytosed cells that produced extra ATP evolved into our mitochondria. Endocytosed cells that could do photosynthesis became the chloroplasts of plants. Not all cells are plants because not all cells with an ancestral mitochondria also ate a cyanobacterium. The fact that plants cells have mitochondria as well as chloroplasts tells us that plant cells developed AFTER cells with mitochondrial ancestors.

But the nucleus may be a tougher nut to crack. It may be that an endocytosed cell good at keeping DNA safe and producing ribosomes became the nucleus, by endocytosis. The data suggests that our DNA is closer to archaeal DNA than bacterial DNA, so it would have been a eubacteria endocytosing an archaea. Or perhaps the archaea invaded the bacterium rather than being endocytosed. The nucleus does have a double membrane and uses some prokaryotic microcompartments to this day, so this could make sense.

But other theories also exist, including one that says an intermediate eukaryotic cell, theoretically called a chronocyte, had developed some organelles on its own or by endocytosis, including a cytoskeleton. This internal structure allowed the cell become bigger, and engulf a cell large enough to evolve into the nucleus.

Another theory uses an evolutionary exception as its basis. Some aquatic bacteria, called planctomycetes (planktos = drifting and mycete = fungus-like), have an organized interior, with something that looks like a nucleus with pores, called a nucleoid. In fact, when they were first discovered, planctomycetes were mistaken for small fungal cells. However, we know they are prokaryotes by DNA sequencing. I thought prokaryotes didn’t have nuclei! Remember that in biology, there is almost always an exception. The planctomycete nucleoid structure suggests that the nucleus may have evolved on its own, without endocytosis.


The planctomycete species, Pirellula (latin for small pear),
is an exceptional bacterium. It has a primitive nucleus
and a stalk that makes it look like a eukaryotic
fungal cell. It was misidentified for a long time, and is
a prime example of why the tattoo above was a bad
idea!
Finally, another theory posits that the nucleus originated from a virus infecting a primitive prokaryote, and this internalized virus forming a nucleus or causing the cell to be predated by another cell. Even though there are different theories for the nucleus, we can see that the three organelles that have double membranes look like they could have been endocytosed cells, that then evolved into the organelles we see today. Endocytosis resulted in symbiosis, so the theory of organelle development is called endosymbiosis.

Endosymbiosis is a cool idea and has lots of support. Besides the double membrane evidence, lets look at how dividing cells get more mitochondria and chloroplasts. These organelles replicate on their own by binary fission, just like bacteria. They can replicate on their own because they have their own DNA. Mitochondrial DNA (mtDNA) and chloroplast DNA (chDNA) are smaller pieces of DNA than nuclear chromosomes, mtDNA and chDNA look much like the small genomes of bacteria. They are also circular pieces of DNA, not linear like our nuclear chromosomes.

By replicating through binary fission, they can be portioned in the dividing cell so that each daughter gets some of these crucial organelles. But it isn’t as if mitochondria and chloroplasts of today look just like the engulfed ancestors. Mitochondrial and chloroplast genomes are greatly reduced from what they used to be.


Serial endocytosis is also called secondary (2˚) endocytosis.
This refers to the movement of DNA from internalized
cells to the nucleus of the endocytosing cell by lateral
gene transfer. This strengthens the symbiotic relationship
between the two organisms until they can be considered
one total organism.
The mitochondria only codes for about thirteen proteins, just enough for it to replicate on its own. The DNA that codes for the rest of the 1500 or so proteins needed for mitochondrial function have been transferred to the nucleus over time. For a discussion of the chloroplast and its horizontal gene transfer to the nucleus, see the posts on C. litorea, the photosynthetic sea slug.

We know that these gene transfers were actual events based on the structure and nucleotide ordering of the mitochondrial and photosynthetic sequences in the eukaryotic chromosomes; they are structured and coded in ways that are typically bacterial. Because of this slow transfer of DNA to the nucleus, endosymbiosis has evolved over time, changing again and again until we got today’s organelles. Therefore, our idea of organelle development is sometimes called serial endosymbiosis theory (SET), because it must have had several different changes through evolution.

Now that we have laid out the evidence and sense for the serial endosymbiosis theory, next week we can talk about some exceptions that show us that that some organisms just can't stick with something that seems to work. Some life just has to take the road less traveled.

For more information or classroom activities on history of life time lines, endocytosis,  serial endosymbiosis theory, evolution of eukaryotes, or planctomycetes, see:

History of life on Earth timelines -

Endocytosis –

Serial endosymbiosis theory –

Evolution of eukaryotes –

Planctomycetes –

Cells Are Great Multitaskers

Biology concepts – compartmentalization, organelle function, cellular biochemistry


This chart represents a portion of the cellular reactions
that are taking place every second in a mammalian cell.
It looks more like a multicolored plate of pasta, but
shows you how complex a single cell is, and remember
that this doesn’t even count all the reactions for one cell
to be able to talk to another cell.
It is hard to estimate the number of reactions that must take place in a cell every second in order to keep a cell alive and performing its jobs(s)...... but I bet it is more than seven or eight.

The typical mammalian cell contains 2000 or more different proteins as well as many thousands of non-proteins (lipids, carbohydrates, and nucleic acids). Each molecule is crucial for carrying out chemical reactions, and each individual molecule is itself produced, modified, and destroyed by chemical reactions.

When I started to think about all this chemical activity, I looked to see if someone had counted, or at least estimated, the number of reactions taking place in the cell at any one time. I got no answer, not even a reliable guess from a credible source.

Think of it in this light, a plant cell has to perform more than twenty reactions to convert one photon of light into the chemical energy that will later be used for the synthesis of glucose. Each of these twenty reactions is occurring simultaneously at least hundredss of times in every chloroplast of the plant cell, and a single plant cell might have more than one hundred chloroplasts. The numbers add up fast, but remember that production of carbohydrate from light energy is just one of thousands of functions of a plant cell. There are chemical reactions occurring every second for all of these functions.

All this chemistry results in perhaps hundreds of thousands or millions of reactions each second, and all taking place within the confines of a cell that is too small to be seen with the naked eye. Wow!

When talking to students, I often use the analogy that a cell is like a factory, producing many different products at the same time. Not unlike a factory, a cell has to perform many functions, such as energy production, product manufacture, oversight and management, transportation of products, quality checks, and cleanup. What complicates matters is that all these different jobs have to be able to occur simultaneously.


I often use the analogy that a cell is like a factory, with
different departments. Other like the cell as a city
analogy. I even had one student make the analogy
that the cell is like a movie set, where the nucleus is
the director, and the plasma membrane is the fence
around the movie lot, etc.   She got an A.
How can a factory, or a cell for that matter, keep all the parts for all the different products, all the different workers, and all the different processes and jobs from messing each other up? A factory does this by setting up departments, where individual jobs take place, and then creating management teams that coordinate the work of the different departments—although to often there is too much management and too little production, but that is another matter.

The business and manufacturing industries stole this strategy from the cell, just as most our good ideas have been copied from nature. The cell uses compartments to increase the efficiency of all its needed chemical reactions. In eukaryotic (eu = true, and karyo= nucleus) cells, the compartments are called organelles (organ = instrument and elle = small), most of which are membrane bound containers.

Remember in our discussion of why cells must be small (It’s All In The Numbers) we said that mixing rate (time needed for a molecule to become evenly dispersed in a cell) and traffic time (time needed for two molecules needed for a certain reaction to find one another) are important for determining the maximum size of a cell.

Membrane bound organelles sequester needed components and create different local environments so that their mixing rates and traffic times are reduced. The result is a cell that is more efficient and can be bigger. This is evidenced by the fact that prokaryotic (pro = before) cells, such as bacteria, don’t have organelles and are about 50 times smaller than eukaryotic cells which have evolved organelles.


The nucleus has two membranes that form an envelope.
The outer membrane is continued as the endoplasmic
reticulum (ER), another vital cell organelle. The ribosome
attached to the ER, so it is easy to see how the organelles
work together to make a functioning cell.
The membranes of organelles look a lot like the membrane that surrounds the cell itself, but organelle membranes are often modified for their particular job. Take the nucleus (Welsh for "kernel of a nut," meaning the central part of a thing) for instance. It has two membranes and nuclear pores that run through both membranes are very specific for what they will let into and out of the nucleus.

The plasma membrane of the cell also limits the passage of molecules, but the nuclear pores are a complex of many unique proteins and this structure that is nowhere to be seen on the cell’s plasma membrane. Just like the membrane of the cell separates what is in the cell from what is outside the cell, the membrane of the organelle separates the needed components of their reactions from all the unneeded components of the cell.

In addition, many chemical reactions in organelles require the membrane as a workbench. Thousands of reactions take place in or across the membrane. This is an important function of many types of organelles, they increase the membrane surface area of a cell without making it bigger.

Some cellular reactions produce or use an intermediate molecule that must be separated across a membrane in order for the rest of the reaction to take place. This is the case for the mitochondrion – the energy producer in eukaryotic cells. To produce ATP (adenosine triphosphate, the chemical currency unit of energy in the cell), the mitochondrion sets up a gradient of protons between two membranes (remember that the nucleus has two membranes also) of the mitochondrion. The energy from the leaking of protons back into the inner space is used to produce ATP. We will talk more about these organelles with two membranes in an upcoming post.


Second messenger systems allow for messages from outside
the cell to be transmitted throughout the cell. There are three
general types, including one for gases like nitric oxide. In all,
there are more than two dozen different signal transduction
cascades, each with its own set of reactions.
Likewise, the outer membrane of the cell has many jobs that require messages to be transferred from one side of the membrane to the other. Called second messenger systems, these reactions are mechanisms to bring messages from outside the cell to the inside of the cell without the need for anything to cross the cell’s boundary.

In some cases, the membrane is not enough compartmentalization. The lysosome is an interesting organelle whose job is to break down many complexes that are brought into a cell and to recycle old organelles so the cell can reuse the parts. To do this, the lysosome contains proteins that can eat up other proteins, lipids, and carbohydrates. Unfortunately, these are the exact same molecules that make up the cell and the lysosomal membrane themselves. So why doesn’t the lysosome digest itself, and the entire cell for that matter?

The protein enzymes in the lysosome work efficiently within a narrow range of acid pH. Therefore, this organelle is acidified when produced. If the lysosome ruptures, the 7.2 pH of the cytoplasm will inactivate the lysosomal acid hydrolases, so the cell is protected. In addition, the lysosome membrane has many sugars stuck to it that act as a buffer between the lipids and proteins of the lysosomal membrane and lysosomal enzymes. There probably is some damage to the lysosome membrane, but repair reactions also help to keep the membrane intact. The cell often has redundant systems for safety.

So, we have seen that many of the organelles function to keep things sequestered in the cell, either for protection, organization, efficiency, or function. However, there are other reasons why organelles are a good idea.


Osteoclasts and osteoblasts are hard workers, so much so
that they needed more than one set of instructions for their
work. The osteoclast above shows multiple nuclei for many
DNA copies. Sometimes separate osteoblasts will join
together to form a multinucleated giant cell.
Organelles increase specificity, both for individual reactions and for cellular activity as a whole. Many cells in multicellular organisms are specialized for a certain function, and their organelles help them carry out this function. For instance, muscle cells are specialized for contraction, and this requires lots of energy. Therefore, they need many mitochondria, but few other types of organelles. These cells might contain 10-100 times more mitochondria than other cell types.

Likewise, osteoclasts (osteo = bone, clast = break) cells break down bone – and yes, you are breaking down and rebuilding your bones every second of every day. This activity requires many proteins to be produced, and one set of DNA instruction housed in one nucleus is often insufficient for the job. Therefore, these cells often have two or more nuclei in order to get the job done.  In these ways, specialization of organelle compartments and combinations allows for specialization of cellular function.


Centrioles are organelles important for the cellular
division. They are also a target for cancer therapy,
since many cancer cells have more than the regular
set of two centrioles.
As we have seen in every topic we have investigated, there are exceptions in the world of organelles. Some organelles are not membrane bound bags that carry things around or house certain reactions. Ribosomes are cellular organelles that make proteins, but they have no membrane. The cytoskeleton elements help the cell hold its structure, help the cell move, and help move other organelles move around within the cell, but they are not membrane bound either. Other cellular components, like the mitotic spindles of the centrioles that pull chromosomes apart when the cell undergoes mitosis are proteins that are present at only certain times in the animal cell. Even more confusing, plant cells divide similar to animal cells, but don’t have centriole organelles.

The take home message is that these organelles, whether membrane bound or not, perform vital services for the cell and make the many cellular reactions possible. The general modus operandi for organelles is that they carry out their functions with in the cell, but one type of organelle is the exception, it’s the traveling organelle.

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For more information on organelles, see:

Organelles –
http://www.teach-nology.com/teachers/lesson_plans/science/biology/cell/
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