through
trisomy
example
distinctive
difficulties
trisomy
lack of
that causes
needs more energy
responsible for
they
held by
form
which revealed
through
contains
forming
and
by
are
some acid
by
DNA sequence to
example
are
which are
to
are read by
they make up
three nucleotides together
are
humans lost
basis of feild
studied in
rest are
without them
known as
like
length of DNA
DNA discovered in 1869
red blood cells
DNA can be extracted
with
that breaks
onto the
facilitates
instead of
is made
where
which is
in
resulting in
which is
facilitated by
through
example
to ensure
this helps
to
since
this way
which is
however
just one gene is affected
of a gene
sequence of
change
which results in
compacted by
which are
for
rest are all
which are
also
consists of
is also
Shape
these make
in a single person
chemical changes are made
known as
assembles the corresponding
DNA backbone
genes also
20 amino acids turn into
Blood as well

DNA

Prokaryotic DNA

is

found in cytoplasm

found in plasmids

double helix

double-stranded

Circular DNA

doesn't contain introns

non-coding regions

coding regions

making proteins

single circular chromosome

not much DNA

lacks transposons

mobile DNA segments

unlike eukaryotic DNA

small and less complex

not tightly packed

nucleoid-associated proteins.

not bound with proteins

no chromatin structure

Double helix

proposed by

James Creek

Watson

Mutations

sequence in the DNA

change of the proteins

can occur in DNA replication

mutations can be inherited

can occur in

chromosomes

alterations

structure

number

gene

nucleotide

is altered

which its influence is low

some diseases

can occur

sickle cell anemia

hemophilia

sex-linked diseases

Cystic Fibrosis

Huntington Syndrome

occurs by errors in DNA replication

Mitosis and Meiosis

Mitosis creates to identical cells

DNA is not degraded

No recovering dead DNA

DNA is replicated and distributed

make new cells

DNA stay alive

it passes on to next generations

Hereditary material

which was determined by

MacLeopd

McCarthy

Avery

Replication

where replication can occur

S-phase

Nucleus of cell in eukaryotes

replication fork

Inside the nucleus

multiple

Through

Transcription

RNA

similar to DNA

with some differences

another nucleoside

uracil

thymine

different sugar

ribose

single stranded

from DNA

Enzymes

DNA Polymerase

addition of nucleotides

growing strand

Helicase

hydrogen bonds

helix is separated

Semiconservative

Other strand

old

One strand

newly formed

2 DNA molecules

2 strands each

Interesting Facts

can be damaged

Chemicals

Radiation

from Various Sources

Hair and skin cells

DNA...

Capable of change

randomly during repliction

Frequency change by mutagens

can be two sets in 1 person

chimerism

Undergoes tiny mutations daily

Don't have DNA

Other types of blood

have DNA

DNA makes RNA

RNA makes protein

no life

not all DNA is genes

only 2% are genes

"Junk DNA"

epigenetics

DNA can be Modified

Human genome

99% identical

6 ft in each cell

3 billion base pairs

30,000 genes

Throughout evolution

over 500 DNA codes

Codes

sequences of nucleotides

genetic instructions for organism

cellular machinery

produce proteins

chains of amino acids

ribosomes

genetics codes in humans

the same

everyone has codes for arms

steps a code goes through

transcription

messenger mRNA

RNA polymerase

RNA processing

modifying mRNA molecule

Translation

proteins are assembled

Protein modification

chain is folded/modified

Transport

cells/outside cells

codon

codes for a specific amino acid

encoded by more than one codon

64 possible codons

Nucleotides

Nitrogenous base

Complementary

Purines

Double ring

Adenine

Guanine

Pyrimidines

Single-ring

Thymine

Cytosine

deoxyribose

Pentose sugar

Pentagonal ring shape

held by

phosphodiester bonds

Consists of

10 hydrogen atoms

1 oxygen atom

5 carbon atoms

forms

Linear

Beta deoxyribose in DNA

Cyclic

used in DNA

phosphate group

Made of

1 phosphorus atom

4 oxygen atoms

held together

ester bonds

base pairs

double ring

single ring

attaches to

5' carbon of sugar

3' to next carbon

pattern of sugar-phosphate

stable structure

based on the work of

Edwin Cargaff

base complementary

"DNA of any species

equal amounts

Adenine

Thymine

Crystal structure of DNA

X-Ray Diffraction

helical shape of the DNA

Rosalind Frank

unify together

base pairs

hydrogen bonds

keeping the two stands

together

complement each other

cytosine

adenine

guanine

thymine

held by

three hydrogen bonds

to separate

held by

two hydrogen bonds

affects

several genes

diseases and/or syndromes

like

Turner

one sex chromosome

characterized by

sterile female

short structure

Down syndrome

chromosome 21

characterized by

in learning

facial features

short neck

Klinefelter

sex chromosome

characterized by

sterile male

long

arms

legs

they all

can be observed

karyotyping

Because they are paired

which are

autosomal diseases