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Hi. You’re on a rock, floating
in space. Have did we get here?
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Well, about 4.5 billion years ago, the earth
was big ball of flaming rocks, constantly
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bombarded by even more rocks from space. Fun
fact! Those rocks probably had some water
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inside them, which has now turned into steam.
Breaking news! The earth is cooling down. Oh yeah,
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did I mention tha- [it’s raining.]
Whoops, everything’s flooded, but hey,
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at least there’s some cool stuff at the bottom,
like hydrothermal vents, which are piping hot
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and filled with a bunch of chemicals, that can
make some very interesting stuff. Wait a minute,
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what the heck is going on here?
[Biology]
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Biology is the study of life, but really,
it’s just chemistry in disguise. I mean
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you and I are basically just a big ball
of molecules that can make funny sounds.
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Carbohydrates give you quick energy, lipids store
long term energy and make membranes, proteins make
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up tissues and nucleic acids make DNA. Also, to
make all the chemical reactions possible, living
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beings, have inside of them a bunch of enzymes.
They’re special proteins that act as catalysts,
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which just means they help chemical reactions
speed up by either breaking down or combining
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one specific thing. For example, lactase
breaks down lactose, the sugar found in milk.
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Ok, so enzymes make life possible
by speeding up chemical reactions,
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but what even is…life? Scientists don’t really
seem to agree, but obviously a cat is different
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from a rock. The cat can produce energy by
metabolizing food, it can grow and develop,
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reproduce, and it responds to the
environment, whereas the rock does not.
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Also, unlike rocks, every living thing on
earth is made of cells, of which there’s
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two main categories: Eukaryotes and prokaryotes.
Eukaryotes have fancy organelles which are bound
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by membranes, like the nucleus, inside of which is
DNA. Prokaryotes, have none of those organelles,
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and the DNA is just kind of chilling
there, like freely floating around.
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This is why Prokaryotes are just
single cell organisms like bacteria
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and archea whereas eukaryotes can form
complex organisms like protists, fungi,
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plants and animals. These are what’s known
as “kingdoms”, which is a taxonomic rank,
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so basically, how we classify different living
things and how they’re related to one another.
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Because there are quite a few species of
life on this planet, and naming them cat,
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dangerous cat and water cat wouldn’t really be
all that helpful, we also give every species
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a unique and unambiguous scientific name
consisting of the genus and the species.
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One thing every species has
in common is homeostasis, aka,
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keeping certain conditions in check, so ya don’t
die. If you feel warm, your body will sweat,
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if you’re cold, your body will shiver.
A cell does kind of the same thing just
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that it balances out concentrations of certain
chemicals. You see, enzymes for example, only
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work in a very specific environment, let’s say at
some specific pH value. If this changes too much,
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the enzymes will denature and won’t work anymore.
To counter this, the cell needs to constantly keep
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up this specific pH value, which is controlled
by the concentration of acid and base molecules.
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Ok. But like, how does the cell do that?
The secret lies in the cell membrane. You see,
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it’s a semipermeable phospholipid bilayer,
okay that’s way too many words, all it is,
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is two layers of these funky looking molecules
with a polar head and a nonpolar tail.
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This allows small molecules like water
and oxygen to slip right through,
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whereas larger particles like ions need special
channels that can be opened or closed, which
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gives the cell control of what goes in and out.
Naturally, particles move with the gradient,
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so from a place of high concentration
to a place of low concentration. Or,
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in the case of water, it can also move to a place
of high solute concentration, so for example salt.
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Welcome to Biology Pro Tips Season 1, tip
of the day: do not drink too much saltwater.
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There’s a bunch of salt in saltwater, in
fact, more salt than inside of a cell,
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which means it will draw water from your cells and
dehydrate you. Yeah that’s it have a great day.
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The process of balancing out gradients is known
as “diffusion” and happens automatically, but,
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by using a little bit of energy, particles
can actively be moved against the gradient.
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The energy comes from Adenosine
Triphosphate or ATP. To be exact,
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the highly energetic chemical bonds between the
phosphate groups can be broken to obtain energy.
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This is kind of important, as
in, every organism and every cell
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needs to make ATP for example, through cellular
respiration which happens in the mitochondria:
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Together with oxygen, glucose, so sugar, is
turned into water, carbon dioxide and ATP.
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This is nice, but it only works if you already
have glucose. Humans are “heterotrophs”. They
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eat food, inside of which is sugar,
which is then broken down into glucose.
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Plants on the other hand are “autotrophs”.
Simply put, they said “screw food, I’ll just
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make my own glucose by staring at the sun”. You
see, plant cells have small organelles called
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“chloroplasts” inside of which is chlorophyll,
which absorbs red and blue light but reflects
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green light, which is why most plants look green.
The absorbed energy from light is used to split
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water and make a special form of carbon dioxide
which can then be turned into glucose and oxygen.
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Okay quick recap, once you have glucose, either
from food or photosynthesis, you can do cellular
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respiration, to get energy in the form of ATP.
Chemically, ATP is what’s known as a nucleotide.
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It has a phosphate group, a five carbon sugar and
a nitrogenous base. You know what else is made of
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nucleotides? Deoxyribonucleic acid, or DNA.
It consists of two strands of nucleotides,
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with the sugar and phosphate groups, but the
actually important part is the nitrogenous base,
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which comes in four flavours: Adenine,
Thymine, Cytosine and Guanine.
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These bases can form base pairs through
hydrogen bonds, where Adenine goes with Thymine,
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and Cytosine goes with Guanine. These bonds
are what holds the two strands of DNA together.
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Okay, but, how the heck does that store
genetic information? I’m glad you ask!
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A “gene” is a section of this DNA
that codes for a special trait,
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by carrying a certain sequence of base pairs,
which is like a recipe for making a protein.
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Why proteins? Because they’re like really
important, they transport molecules,
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act as enzymes and determine the way you look.
For example, the difference between brown and
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blue eyes is the amount of a pigment called
“melanin” in the cells of the iris. The OCA2
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Gene codes for “P-Protein” which we believe
controls the amount of melanin in cells,
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meaning that the proteins made from this gene,
could be what determines your eye colour.
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Cool! There’s just one issue: Your DNA
and its information is in the nucleus,
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but proteins are made in organelles
called the ribosomes. How do we get the
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information from A to B? The answer is RNA.
It’s kind of like DNA, just that it’s most
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often a single strand, it uses a ribose instead of
deoxyribose and instead of Thymine it uses Uracil,
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which makes it less stable, but that’s besides
the point, here’s what RNA actually does:
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Let’s say you want to make the protein
coded for by this gene. An enzyme called
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“RNA polymerase” will split the DNA and make
a strand of RNA with the complementary bases,
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essentially copying the information from the
DNA to the RNA. This is called “transcription”.
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The new strand is called messenger
RNA or mRNA, because it carries this
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message out of the nucleus to a ribosome.
Remember how I said that a gene is like a
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recipe for a protein? Well, on the mRNA, which
carries the same base sequence as that gene,
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every group of three bases, which is called
a “codon”, codes for a specific amino acid,
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which are the building blocks for proteins.
Welcome to Biology Pro Tips Season 1, if you want
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to decode a sequence of RNA, there is actually a
chart for that! Yeah that’s all have a great day.
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These amino acids are carried by special
molecules called transfer RNA or tRNA,
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which have a unique anticodon that can only
attach to its matching codon on the mRNA.
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The job of the ribosome is to read over codons on
the mRNA and attach the matching tRNA molecules,
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which then leave behind their amino acid. As the
ribosome moves along the mRNA and attaches more
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tRNA, which happens a couple thousand times, the
amino acids combine into a “polypeptide chain”,
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which is just a really long chain of
amino acids, that can be bunched up,
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creased, smacked and folded into a protein.
Okay, let’s recap: A gene is copied onto mRNA,
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which is then used to build proteins
by assembling a chain of amino acids.
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Aka transcription and translation.
Hey, this genetics stuff is pretty
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cool, can we learn more? Absolutely.
Oh yeah did I mention that you have, like,
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a bunch of DNA? You have about 20000 protein
coding genes, each thousands to millions of
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bases long, and that only makes up around 1% of
your entire DNA, the rest is just non-coding.
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PLUS, almost every cell in your body contains your
entire genetic code, but genes can be turned on or
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off depending on the cell, which is good, because
otherwise your brain cells might just start
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making stomach acid, which would not be good.
FUN FACT! If you were to stretch out all the
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DNA of just one single cell, it
would be about 2 meters long.
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Wait a minute, how does that fit into a
microscopic cell? Well, if you were to look inside
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the nucleus, you wouldn’t find the DNA floating
around like this or even this, no, you would
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actually find lots of these worm looking things.
To be exact, DNA is coiled up around Proteins
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called “Histones”, which are then condensed into
strands of Chromatin, which are then coiled up
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even more to make tightly packed units of DNA
called “Chromosomes”, which kinda look like
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worms. Different sections on a chromosome carry
different genes, and the entire human genome is
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split amongst 23 different chromosomes, although
every body cell has 2 copies of every chromosome,
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one from the mother and one from the father.
For most chromosomes, the two copies are
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said to be homologous, meaning that they carry
the same genes in the same location. However,
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the two versions of a gene can be different,
so the mother’s gene could code for brown eyes,
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while the father’s gene codes for blue eyes. These
different versions of a gene are called “alleles”.
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For most of your genes, you have 2 alleles, one on
each chromosome from either parent. These alleles
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can be dominant or recessive, which determines
which of them is expressed. For example,
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brown eye color is a dominant trait, which
is shown by an uppercase B, whereas blue
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is recessive, which is shown by a lowercase b.
All this means, is that if you have the dominant
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brown allele, you will have brown eyes, no matter
what the second allele is. Only when there are
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two recessive alleles will it be expressed.
With this knowledge, we can predict the future!
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Let’s look at how this trait is
inherited from parents to children:
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Both of these parents have brown eyes, but
also have a recessive blue allele in their
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genotype. Every child receives one allele
from each parent randomly, so these are the
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possible combinations for the children.
Most combinations contain the dominant
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brown allele, so the child will have brown eyes.
But, there is a small chance that a child gets
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two recessive alleles and has blue eyes, even
though both parents had brown eyes! You see,
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it’s what’s on the inside that counts.
Alright, that’s cool, but reality is not always
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so simple. Some genes are not fully dominant, but
not fully recessive either, which means that the
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phenotype, so the appearance, appears to mix.
Crossing a red and a white snapdragon, where
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red is “dominant” and white is “recessive” gives
you a pink phenotype which is somewhere inbetween,
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aka intermediate inheritance. Or, crossing
a brown and a white cow where both colours
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are dominant could give you spotted cow, so both
phenotypes are expressed equally, aka codominance.
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Hey remember how I said almost all
chromosomes are homologous? Well,
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there’s one exception: the sex chromosomes.
Females have two big X chromosomes, whereas
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males have one X and one smaller Y chromosome.
These are partially homologous at the top,
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but since the Y chromosome is so small,
it’s missing genes that are present
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on the lower part of the X chromosome.
These genes are called “X-linked genes”.
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If one of these genes is a recessive trait like
colour blindness, males are stuck with that trait,
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whereas females probably have another
dominant allele, to override it. This
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is why most colourblind people are male.
Now, for genes to even be passed on,
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the body has to make new cells which can
inherit the genes. There’s two main mechanisms:
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Mitosis, which is how the body makes identical
copies of body cells to grow and repair tissues,
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and Meiosis, which is how the body
makes gametes, so sperm and egg cells.
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Mitosis starts with a diploid cell, so a cell with
two sets of chromosomes. These chromosomes consist
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of one chromatid, which has to be replicated
for the new cell. After replication is when
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you see the familiar X shape consisting of
two identical sister chromatids. These are
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split into two identical diploid cells, with two
sets of chromosomes consisting of one chromatid.
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Meiosis also starts with a diploid cell, but
after replication, the chromosomes comingle
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and exchange genetic information in a process
called “crossing over”. The cell is then split
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into two non-identical haploid cells. These
have one set of chromosomes, but they still
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consist of 2 sister chromatids. These cells split
again into 4 genetically different haploid cells,
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where each chromosomes has one chromatid.
Meiosis produces haploid cells, so that when two
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gametes combine into a fertilized egg or “zygote”,
it again has the correct number of chromosomes.
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This is cool, but, cell division is only a tiny
part of a cell’s entire life cycle. Most of its
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time is actually spent in interphase, aka just
chilling. All it does here, is grow and replicate
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all of its DNA, so that it actually has enough
genetic material and size to divide in M-Phase.
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There’s multiple checkpoints in the cell
cycle which are controlled by proteins
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like p53 or cyclin to check if the cell is
healthy and ready to reproduce. If a cell
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is not quite right, it’s either fixed
or it destroys itself, which is called
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“apoptosis”…or at least, that’s what it should do.
Normal cells replicate until there’s no need to,
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but some cells just keep going. This is because
they don’t respond correctly to these checkpoints
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and end up replicating out of control and
functioning wrong, which is also known as cancer.
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This damaging behaviour is often a result of a
gene mutation, which is a change somewhere in the
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base sequence of a gene. This can happen during
DNA replication, when a single base is changed,
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left out or inserted into the original sequence.
This often changes the protein coded for by that
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gene and let’s just say that
change is often not optimal.
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Another type of mutation happens in chromosomes,
where entire sections of DNA could be duplicated,
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deleted, flipped around or transferred between
chromosomes. The most famous chromosomal mutation
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is probably when the 21st pair of chromosomes
has an additional copy, so that there’s 3
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instead of 2. The result? Down syndrome.
Mutations might seem like a bad thing,
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but actually, they can also be neutral
or even beneficial. For example,
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a species of yellow grasshoppers might
mutate and become green, which makes them
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blend in with the grass and get eaten less.
Over time, you can expect to see more and
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more green grasshoppers, as their fitness
has increased. Not that kind of fitness,
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fitness as in, they can have more
offspring, because they get eaten less.
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This is natural selection and the driving
factor behind evolution, as the poorly adapted
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species gets selected against and the fittest
species, which has adapted to the environment,
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survives and and has the most offspring,
passing down the trait that made them survive.
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If you think adaptation is cool, yes,
but also it kind of sucks. You see,
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humans can get sick from bacteria or viruses,
but nowadays, we have medicine that works. Good!
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However, what if the bacteria mutates and
suddenly, the medicine doesn’t work anymore? Well,
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that’s kind of exactly what is happening,
aaand we have no clue how to fix it. So, yeah.
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Oh yeah by the way, one thing many people confuse
is bacteria and viruses, and NO, they’re not the
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same. Bacteria are prokaryotes, so they consist
of a single cell which can reproduce on its own,
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and we treat bacterial infections such as
strep throat and tetanus with antibiotics.
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Viruses are not made of cells, in fact,
we’re not even sure they’re alive. They
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share some signs of life, but they can only
reproduce inside a host, and they don’t grow,
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so it’s not really alive, but it’s not dead
either, it’s more of non-living kind of thing.
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Also, you cannot treat viral infections with
antibiotics, most of the time you just have to
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chill out and let your immune system do its thing.
Now you might think bacteria are a bad thing, but
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actually, you have millions good bacteria inside
your gut. The live in symbiosis with you, so you
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give them food, and they help you digest it.
Speaking of digestion, your body is made of
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many complex organ systems that work
together to make sure you don’t die,
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and I know what you’re thinking. Actually
I don’t, but I know how you’re thinking.
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The nervous system, consisting of nerves,
which connect to the spinal cord and lead
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to your brain, is made of cells called
“neurons” which can conduct electricity
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along this long tube called the “axon”.
Anything you see, think and feel, it’s
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all just electrical signals going to your brain,
and your brain telling your body how to respond.
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To be exact, the signals are called “action
potentials” and happen at the same strength
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and the same speed every time, so
the only difference between “hey,
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I’m a little cold” and “OMG I AM ON FIRE” is
where it happens and how frequent the signals are.
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When a neuron is just chilling, the axon is
more negative on the inside than on the outside,
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because there’s an unbalanced amount ions. This
causes an electric potential of about -70mV.
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When there is a stimulus, signalling molecules
called neurotransmitters dock onto ion channels on
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the axon and open them, letting the ions flow and
changing the electric potential around that area.
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Now, action potentials are all or nothing.
A small stimulus won’t really do anything,
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but, if the potential exceeds about
-55 mV, boom, action potential.
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Ion channels around the stimulus
open and ions rush into the cell.
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This causes the charge distribution in that
section of the axon to reverse for a split second,
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which is called “depolarisation”.
The ion channels that are next to
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this area are influenced by this and open as well,
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which causes a chain reaction and sends
the signal all the way down the axon.
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Some neurons have a myelin sheath made
of Schwann cells, which insulate the
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axon and only leave tiny gaps called nodes of
ranvier. If there’s a stimulus, the charges
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can “jump” across the nodes which transmits
the signal way faster than a normal neuron.
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But either way, at the bottom, the electric signal
reaches a terminal button, which connects the
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current neuron to the dendrites of the next. If
you zoom in, you’d notice that the two cells don’t
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even touch, there is actually a small gap. This
is once again where neurotransmitters come in:
[16:24] (984.56s)
Once the button is depolarized, tiny packages
of neurotransmitters get released, and bind
[16:28] (988.52s)
to receptors of following dendrite, either
blocking it from doing anything or causing
[16:32] (992.32s)
another action potential, which repeats the cycle.
Hmmm. Something in my brain’s telling me that you
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should definitely subscribe, and also, if you
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