Everything In Bio Flashcards

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1
Q

What is the molecular amino acid building blocks?

A

The four elements to an amino acids is an amino group (NH2), an carboxyl group (COOH), then a hydrogen connected to a center carbon and last an R-chain, each specific to the 20 different amino acids.

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2
Q

How many essential amino acids are there out of the 20 that we use in making proteins?

A

There are 9 essential amino acids that the body does not make, and ergo there is 11 non essential

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3
Q

What is the promotor of a gene?

A

The promotor of a gene is where the transcription will start copying in terms of transcription. Ahead of all genes there is an area on the DNA that says where the transcription will start. This is the area that is called the promotor

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4
Q

What is the enzyme complex RNA-polymerase? And what jobs does it got?

A

The enzyme complex RNA-polymerase is an important protein complex that have a very important role in making protein. The jobs that it’s involved with is first that one of the enzymes hooks on to the promotor, it does this with help of transcription factors that identify and latch on to the promotor.
RNA polymerase also separates the DNA. Then another RNA polymerase can come and make an mRNA-thread

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5
Q

mRNA is made as the complementary unit of the DNA strand it gets copied from, but which end does the DNA strand start from, and then which end does the mRNA start with?

A

Since we got two ends, one 3’ end and one 5’ end, that start in each corner, and since DNA gets transcripted from the 3 to 5 end, then the mRNA goes from 5 to 3 end.

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6
Q

How fast does RNA-polymerase make nucleotides?

A

It makes around 50 nucleotides per second. Which is kinda intense

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7
Q

What is an intron, an exon and spliceosome?

A

A gene contains the recipe for the protein, but inside that gene there is areas that do code for the protein (exon(express)) and then there are areas that fills in the gap between (intron). In order to make the finished protein the areas that do not code needs to get eliminated. This is where spliceosome comes in. Spliceosome comes in and cuts open the pre-mRNA (the first mRNA) and cuts out the intros, leaving only the expressed gene left, the exons, which then is the finished mRNA.

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8
Q

The first part of modifying the pre-mRNA is where the 5’ and 3’ ends gets attachments, what happens?

A

In the 5’end enzymes comes and give it a phosphate group, this group is called the 5’cap. And in the 3’end it gets a tail of nucleotides with the base adenin, this tail is called the 3’poly-A. These modifications will protect the ends of the mRNA in cytosol in the process of translation, also it helps the ribosome connects properly to the mRNA

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9
Q

What is start kodon?

A

After the sub unit of the ribosome locks on the 5’cap, then it rolls on the mRNA until it finds the start kodon, which is the nucleotides AUG. Here it can start the protein synthesis and locate the complemtary tRNA’s. AUG is the antikodon UAC, which is tRNA(met) the amino acid mentionin

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10
Q

What is a stop kodon?

A

A stop kodon is the place on the mRNA that lets the ribosome know that the protein synthesis is complete. It’s one of three stop kodon; UAA, UAG or UGA, these do not have an anti kodon to match, instead a protein called a stop factor connects to the stopkodon and the whole ribosome complex detached from itself.

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11
Q

What is tRNA-synthesiser?

A

The tRNA-synthesiser is an enzyme that recognises the anticodons that the different tRNA brings to the ribosome, and thereafter connects it to the right amino acid

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12
Q

How many amino acids is a protein typical made up of?

A

A protein is typical made up of around 100 to 600 amino acids. But, some proteins are more complicated than others, and therefore use multiple amino acids chain, and like glutamatdehydrogenase use around 40 amino acids chains and around 8300 amino acids

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13
Q

Protein get their unique shape through specific amino acids and the folding of these acids. What are the four stages of protein folding?

A
  1. Primary structure. Here we gain the amino acids and the amino acid chains.
  2. Secondary structure. This is where the first folding happens, they fold in either beta-plates or helix structures.
  3. Tertiary structure. This is where the beta plates and the helix structures link up and begin folding thereafter.
  4. Quaternary structure. This is the finished protein
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14
Q

What are prion diseases?

A

Prion diseases like Creutzfeldt-jacobs disease is diseases where protein folding isn’t correct. These misshaped proteins can make other proteins fold like them, in a wrong way. Usually these get destroyed rather quickly but sometimes they don’t and this is where diseases can happen. Like mad cow disease, this is just a missfolded protein in the brain

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15
Q

What is a transcription factor?

A

A transcription factor is a protein that determines how often a gene will get expressed.

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16
Q

What is the difference between enchancer and silencer?

A

An enchancer is a area in DNA when bound by transcriptions factors will increase the activity of that gene.
A silencer on the other hand are then areas of the DNA when transcription factors attached will decrease the activity of said gene.

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17
Q

What’s the difference between a chromosome mutation and a gene mutation? And also, what is a point mutation?

A

Chromosome mutations involve the whole or a big part of the chromosome, while gene mutations is just changes to the order of bases that gets altered. A point mutation is where only one basepar gets mutated.

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18
Q

Which three ways does mutations happen?

A

Substituting, where it just get rearranged. Like a basepar gets swapped out for another basepar.

Insertion, where something gets added in. When one or multiple basepars gets added in.

deletion, where something gets removed. Where one or more basepars gets removed.

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19
Q

What are mutagens?

A

Mutagens are factors, or agents like radiation or chemical substances that can cause mutations.

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20
Q

What are cell differentiation?

A

Cell differentiation is where the cells gets the specific field of specialty, like some gets to be a muscle cell, or like a nerve cell. But also tissue and blood cells. This happens via which genes gets expressed.

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21
Q

Which enzyme separates the double helix structure?

A

Enzyme helikase

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22
Q

At the beginning of DNA replication, after the helicase splits the two strands, the next enzyme is primase, what does it do?

A

The enzyme primase makes the entry point to where to replication will start, this is called the primer. Eukaryotic cells have multiple start location, while prokaryotic only have one

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23
Q

The three enzymes helicase, primase and complex DNA-polymerase makes the three starter protein in DNA replication. What do they do?

A

Helicase is the one that opens up the double helix, making the replication possible.
Thereafter primase makes a primer marking the place to start, goes from 5’end to the 3’ end. The primer are around 5 to 10 nucleotides.
Then the enzyme complex dna-polymerase starts the replication process, going from the 5 end to the 3 end. There are multiple DNA-polymerase that works on the replication.

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24
Q

What enzyme glue together all the new fragments in the replication process?

A

The enzyme DNA-Ligase glues them together, this enzyme works from the 3 end to the 5 end

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25
Q

When errors occur in the replication process, like a G instead of T to the complementary A, which enzyme complex fixes the error?

A

A part of the enzyme complex DNA-polymerase fixes error that occurs. This enzyme complex does multiple things, so not only does it make a complementary thread but it also fixes erorrs

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26
Q

How many autosome and sex chromosomes do a person have?

A

A person has 44 autosome (22 pairs) and 2 sex chromosomes (1 pair)

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27
Q

Are male sex chromosomes homogolous?

A

No, because they have one X chromosome and one Y chromosome, a female on the other hand has a homogelous sex chromosomes, because they have two X chromosomes

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28
Q

What’s a telomere?

A

A telomere is the end of each chromosomes, this spot protects the chromosomes in terms of replication. And each replication the telomere gets shorter. This is why we can assess a person age from this.

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29
Q

Mitosis is separated by 5 phases and then cytokinesis. Describe the 5 phases with simple terms.

A

Proface: this is where the two chromosomes condenses to the point that we can see it with a light microscope. Also the spindle apparatus which are made up of microtubule starts getting made.
Prometaface: nucleus gets dissolved and the spindle apparatus attached to the sentromeres are the sister chromatids. These also moves towards the middle of the cell.
Metaphase: the chromosomes gets arranged each on their own.
Anaphase: the chromosomes gets separated, the spindle apparatus shortens and pulls the sister chromatids to each of ends. Results are two full sets of chromosomes at each of the ends.
Telophase: the spindle apparatus disappears and then two nucleuses gets made for each of the future cells. They decondenses and they start looking more like the linear strands that they are most of the time.
Then cytokinesis comes and separates all of the organelles and nucleuses and voilà, we have to diploid cells that soon goes into interphase again, where they will spend most of their time

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30
Q

In cytokinesis, what are the difference between plant and animal cells?

A

In plant cells there are multiple vesicles that contains material to cell walls that melt together and form a cell plate in the middle.
Animal cells on the other hand there almost like a string that winds itself up around the middle and separates the cell into two

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31
Q

What are gender cells called?

A

gametes, and these are diploid

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32
Q

What are meiosis?

A

Meiosis is the process of production of gender cells. This happens when the plant or animal produces a diploid cell that then separates into haploid gender cells. This process is a form of meiosis

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33
Q

What phases do meiosis have?

A

Like mitosis they have an interphase where in the s-phase the DNA gets replicated. After that we have meiosis 1 and 2.
These are like mitosis compared of the same 5 phases.
Proface, prometaphase, metaphase, anaphase and telophase.
Also cytokinesis happens after both meiosis I and meiosis II

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34
Q

How many times does cytokinesis happen in meiosis?

A

There are two instances of cytokinesis in meiosis, one after meiosis I and one after meiosis II

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35
Q

How many haploid cells gets made from meiosis?

A

There will be made four haploid cells of one instance of meiosis. This is because the one cell (haploid) gets into cytokinesis in meiosis I and then make two haploid cells, and then the two cells will go into cytokinesis and make four haploid cells (gametes)

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36
Q

What happens with the chromosomes in meiosis I and in meiosis II

A

The same process in the phases happens with the spindle apparatus happens and separation process.
But in meiosis I the homologous chromosomes gets divided into the two cells, and then in meiosis II the sister chromatids get separated. Unlike in mitosis this only takes one process, but this also only creates two cells instead of four.

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37
Q

When does the crossover happen and what does it mean?

A

The crossover in meiosis (only in meiosis) happens in prophase I, and this is where sections of the chromosomes gets swapped between the sister chromatids so they get a bigger variety.

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38
Q

What is homologous chromosomes?

A

It’s the identical match of a single chromosome, we have 22 autosomes chromosomes, each of these are homologous and then we have one pair of sex chromosomes. If a person is a female then it’s homologous, but if it’s a male then it’s not, XY.

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39
Q

What is the locus of the gene?

A

The locus of the gene is the place that specific gene is located in the chromosome.
When we have two homologous chromosomes, two pair, they will code for the same things, meaning that the gene of a specific thing, usually protein is located at the same place on both the chromosomes

40
Q

What is phenotype?

A

Phenotype is what will come to expression in terms of properties. These properties can be both visible and invisible, like I have blue eyes or how I break down lactose

41
Q

What is genotype?

A

Genotype is the genes that the DNA have, with both its alleles or variants, it’s what come before phenotype, which is what genotype that is expressed

42
Q

What is Mendels first heritage law?

A

Each gene variant(allele) separates at random and therefore there is equal chance for that to be passed on to the next generation

43
Q

Mendels second heritage law?

A

Different gene pairs gets distributed to the next generation independent from each other. This only applies to genes sitting on different chromosomes

44
Q

What doesn’t follow Mendels law of heritage?

A

Most of the heritage diseases and attributes. A attribute is controlled by a complex interaction between multiple genes and the environment

45
Q

What is monohybrid inheritance?

A

This is where there is one attribute that gets decided by one gene pair gets inherited, like the flower color of peas.

46
Q

What is the difference homozygous and heterozygous?

A

Homozygous means that there are two identical alleles of the same genotype. While heterozygous means that there are two different alleles of the same genotype. So TT and Tt

47
Q

What’s the different between recessive and dominant gene?

A

Dominant genes will always express them self over recessive genes. So if you have a heterozygous dominant, meaning you have two different alleles of the same genotype, then the dominant gene will become the phenotype Tt = T gets expressed

48
Q

What is dihybrid inheritance?

A

Dihybrid inheritance is where to attributed where both gets decided by one gene pair

49
Q

What is connected genes?

A

Connected genes means that there are genes that connected to the same chromosome and these will then be inherited together

50
Q

Hva tilsier mendels andre lov hvis gener arves uavhengig fra hverandre og det finnes gener som ligger på samme chromosom, som bananfluene sin farge og vinge?

A

Mendels andre lov tilsier at gener arves uavhengig fra hverandre og derfor har lik sjanse å bli arvet til neste generasjon. Men denne regelen gjelder kun når gener ikke er på samme kromosom. Noen gener vil bli arvet med hverandre.

51
Q

What’s special about the inheritance of sex chromosomes?

A

Recessive chromosome errors on X chromosomes will always be a phenotype when its male.

52
Q

Genes and inheritance is complex. Usually when we think about genes we think that one gene pair decide one attribute, and one of dominant while the other is recessive, it’s usually multiple gene pairs involved in the inherited attributes. How does the scale look like in terms of the dominant gene interaction between each other?

A

It’s called the scale of dominance. On the one end it’s complete dominance, and the other is codominant, in between we have incomplete dominance

53
Q

What differs from incomplete dominance and codominance? See it in light of lion mouth flowers, where we cross two homozygous genes, one FF red and one ff white. When they breed they get a 1:2:1 where two is pink. This is incomplete dominance.

A

In incomplete dominance we will get a middle variant, like the lion mouth flower. While in codominance we will only see one or the other color, it’s both and.

54
Q

In the blood system ABO what does the letter point too?

A

A and B points to two carbohydrates that sits on the surface of the red blood cells. While O do not have this carbohydrate.

55
Q

People who have the blood type AB is where on the dominance scale?

A

AB is codominant. Meaning that the genes for these carbohydrates on the surface gets expressed equally.

56
Q

Since the blood type O doesn’t have any carbohydrates on the surface it can do what?

A

Since the red blood cells don’t have any carbohydrates on it’s surface it won’t be repelled for having the wrong one, basically it’s an universal blood giver meaning A, B, and AB can receive it.

57
Q

When one gene pair has more than two variations it’s called multiple gene variations, give an example of this

A

The blood system ABO. This attribute is contributed by a single gene, and while looking that ABO you would think that we have three types. Men in reality we have 4 phenotypes.

58
Q

What are lethal genes?

A

Lethal genes are gene variations that leads to death when they get expressed, usually in the fetus-stage.

59
Q

What are pleiotropic genes?

A

When one gene codes for multiple attributes.
Example the gene for chlorite channels, where these are important in respiration and digestion. This can also cause cystic fibrosis.
Another pleiotropic gene is the gene OCA2, this gene is among the genes that codes for the eye colour, hair colour and skin. When this is turned off it causes people having red eyes, white hair and skin.

60
Q

What is epistasis?

A

Epistasis is where one gene phenotype is masked, suppressed or expressed by the appearance or not of another gene or multiple.
Another definition is a gene is epistatic when it’s presence suppresses the effect of another gene at another locus.

61
Q

What is epigenetic?

A

Epigenetic is where we look at changes in geneactivity but without changes in the genetic code. Like attributes comes into light because of cell divisions and reactions to the immediate environment. These have also been shown to give effects in the long-term

62
Q

What is DNA-metylation?

A

DNA methylation is where a metyl group (CH3) attaches at the 5’end carbon group, usually a cytosin, and that cytosin is usually next to a guanine. When there are multiple methylated group close together that gene usually is less active. This is why it’s connected to epigenetic, because we don’t change the genes, we just choose which one to activate. This process has a big impact on cell differentiation, and choosing which gene to activate and not.

63
Q

What is histone modification?

A

Histone modification is where histones, the protein that DNA gets wrapped around with to reduce space. These histones have a tail and on that tail enzymes can choose to put on a chemical group, which is usually acetyl.
These chemical groups decide how tight the DNA gets packed, and loosely said the more histone modification in an area, the more easily the DNA is to get expressed.
Like methylated and histone modification, both gets inherited.

64
Q

Name another epigenetic mechanism involving RNA.

A

Sometimes a gene can gets turned on and then transcribe a product that maintains the activity in the gene, even if the signal is not in place. Descendants of the cell where it was original turned on, inherit the gene activity, even if the original signal to turn on the gene isn’t in place.

65
Q

Name three epigenetic mechanism

A
  1. DNA methylation
  2. Histone modification
  3. RNA molecules that signal
66
Q

What is imprinting?

A

Imprinting in the epigenetic world, is that for multiple genes the phenotype for the offspring is determined if the gene is inherited from mom or dad. The genes is therefore characterised different from mom or dad. This is called imprinting

67
Q

What is X-deactivation?

A

X-deactivation happens to females to the sex cell, because they have a homologous set one of them needs to be inactivate, more or less so that complications doesn’t occur.

68
Q

What’s the common denominator of genetic diseases?

A

All of them on one or another way are caused by changes in or on the DNA

69
Q

Mutation in genes that codes for protein can lose its normal way of function, what two main categories can it be separated too?

A

Those that don’t work at all and those that do their task wrong

70
Q

Mutation happens all the time, but why is it more dangerous for the person and offspring if the mutation hits a sex cell instead of a autosome cell?

A

Mostly because in autosome cells we have a lot of inactive parts of DNA, and also most of the mutation are harmless, but considering the place and mutation anything can happen. But generally if a mutation hits a sex cell and this sex cell is the one that take parts in fertilisation then it will most likely affect all of the cells in this new individual.
Some of these mutation will also keep getting inherited by future generations.

71
Q

Name three ways for errors in the DNA can happen

A
  1. External forces, like radiation or mutagens
  2. Copy mistakes
  3. Mistakes in the dividing of chromosomes in meiosis
72
Q

Name three recessive inherited diseases

A

Cystic fibrosis
PKU (føllings sykdom) engelsk er phenylketonuria
Angelman syndrome

73
Q

Name three dominant inherited diseases

A

Huntingtons disease
Neurofibromatosis
Osteogenesis imperfecta

74
Q

Name three sex gender inherited diseases

A

Different type of bleeders disease
Colourblindness
Duchennes muscledystrophy

75
Q

Name three chromosome deviation diseases

A

Down’s syndrome
Turners syndrome
Klinefelters disease

76
Q

Recessive inherited diseases are often connected what? And how does these manifest

A

Recessive inherited diseases are often connected to mutations that gives non-functional proteins.
Recessive inherited diseases manifest because both of the genotype of the protein are mutated. For a person to be sick and not a carrier of these kind of diseases that person would need homozygous recessive genotype. If it’s heterozygous then the healthy gene would be able to maintain the proper gene.

77
Q

In Norway how many are afflicted by cystic fibrosis?

A

1 in 25 persons are afflicted by cystic fibrosis

78
Q

What are cystic fibrosis?

A

Cystic fibrosis is an autosomal recessive inherited disease. Cystic fibrosis causes abnormal salty sweat and abnormal mucus production. The gene is on chromosome 7, and the gene that cystic fibrosis fucks up are involved in chloride channels, which has its main job in transporting chloride ions through the cell membrane.
There are multiple variants of the disease, this is only because there is different degree of severity of the functionality of the gene.

79
Q

PKU, føllings disease, phenylketonuria is a recessive autosomal inherited disease that does what?

A

PKU/phenylketonuria is an autosomal recessive disease that inhibits the development of the nervous system.
Phenylketonuria afflicts chromosome nr 12 and is a metabolic disease that will inhibit the nervous system.
The gene that’s afflicted codes for the enzyme phenylalanine hydroxylase, this enzymes job is breaking down the amino acid phenylalanine, when this doesn’t occur and the congestion(opphopning) of the amino acid is toxic to the cell.
The disease can be maintained if it’s detected at an early age and eat the correct diet

80
Q

What is angelman syndrome?

A

Angelman syndrome is a recessive chromosome disease that happens at chromosome 15. This syndrome causes a severe degree of development disability. Delayed development of motor and cheerfulness.

81
Q

What is imprinting?

A

Imprinting is something that probably occurs because of variety reasons and protecting and isolating the activity of the genome. Imprinting is a form of DNA methylation, and this we know causes the genes to be inactive. Imprinting happens different from mom and dad, the effect of this is that both gene variants in a gene pair isn’t both active or inactive.

82
Q

Explain autosomal dominant inherited diseases

A

Autosomal dominant inherited diseases is where it’s enough to have one of the two alleles of the gene to make it express itself. So if a person have one broken allele and one healthy then the broken one will get expressed.

83
Q

If we have an autosomal dominant disease, like Huntington disease, and then a mother who is heterozygous of the this disease, and a father who is homozygous recessive what will the four children become?

A

The mother is Hh and the father is hh, then the children will become hh, hh, Hh and Hh. Making one of two of the kids have Huntingtons disease.

84
Q

What is Huntington’s disease?

A

Huntingtons disease is an autosomal dominant inherited disease that affects the nervous system thereafter it will cause brain loss. The symptoms don’t appear before the age forty to fifty and normally a person dies within 10-15 years after the first symptoms.
The disease sits on chromosome 4.

85
Q

What’s special about lethal dominant genes, like Huntingtons disease?

A

Lethal dominant diseases only gets inherited if the gene leads to death at a relative adult age, because that way the sick gene may already have been transferred over to the next generation. If the lethal dominant gene had killed the patient at an early age then the gene wouldn’t have been transferred and would have stopped right there at history.

86
Q

Gendered inherited diseases are mostly what?

A

Recessive. This high light the cases that women need two sick alleles on the gene locus to be able to get sick(two sick X X chromosomes), if not they are usually a carrier. Men on the other hand only need one sick gene on the X chromosome because the other gender chromosome is a Y and therefore cannot compensate. This is also why gendered inherited diseases are more common in men than in women. A male can only be healthy or sick, not a carrier.

87
Q

What is bleeder sickness?

A

When one gets a cut and the person starts to bleed homeostasis kicks in. This mechanism is for to close wounds and bleedings, in this process we would need a lot of different coagulant factors to make the blood harden and eventually close the wound. When a person is missing these factors the blood will not harden and we would end up in excessive blood loss. These coagulant factors sits on the X chromosome (gendered) and is a gender inherited sickness. More men than women therefore gets affected

88
Q

What is chromosome abnormalities?

A

Chromosome abnormalities comes in two main groups, numerical and structural abnormalities.
In numerical there is either missing a chromosome or there is one too many.
In a structural chromosome abnormality the chromosomal structure is skewed in one way or another. There are five structural errors to be happen.

89
Q

In structural chromosome abnormalities there are five ways for errors to happen, name the five ways

A
  1. Deletions. A part of the chromosome is missing or is deleted.
  2. Duplications. A portion of the chromosome is duplicated resulting in extra genetic material.
  3. Translocations. (Two ways). A portion of one chromosome is transferred to another chromosome. Either two parts have exchanged, one from each chromosome. Or an entire chromosome has attached to another centromere (robertsonian translocation).
  4. Inversions. Inversions happens when a portion of the chromosome has broken off and turned upside down and then reattached itself.
  5. Rings. This is where a portion of the chromosome has broken off and formed a circle or a ring. This can happen with or without loss of genetic material.
90
Q

Chromosome abnormalities usually happens in?

A

Chromosome abnormalities usually happens in meiosis as in the egg or the sperm as an accident.
It can also happen in mitosis.

91
Q

Down’s syndrome is usually causes by chromosome abnormalities, but is it possible to be inherited?

A

It is possible to be inherited, but that’s only when people with Down’s syndrome gets kids.

92
Q

In what three ways can a person be born with Down’s syndrome?

A
  1. Trisomy 21. This is the most common one with about 95% of all people with downs have this form of chromosomal abnormality. Trisomy 21 happens when a person if born with three chromosome nr 21 instead of 2. This is a numerical abnormality.
  2. Translocation Down syndrome.
    Translocation Downs syndrome is where a extra part or a whole chromosome 21 is present but is attached(translocated) on another chromosome. 3% affected.
  3. Mosaic Down’s syndrome. This is where only some of the cells chromosome 21 have an a trisomy, but not all. This may cause the child to have fewer features of the condition than a normal trisomy 21 case. 2% of people with Down’s syndrome are affected.
93
Q

What’s a factor for normal women to have a higher chance of giving birth to someone with Down’s syndrome?

A

Age. A higher age of a women drastically increases the chance of giving birth to a person with Down’s syndrome. This is because women are born with a set number of eggs, while men produce sperm throughout most of their lives.

94
Q

In turners syndrome is a chromosome abnormality where what happens?

A

Turners syndrome are people that are born with only have one X gender chromosome, these are women and are often born with completely norma mental functions but are stunted in growth (short height).

95
Q

Klinefelters syndrome is also a chromosome structural error, but what happens?

A

In Klinefelters syndrome have three gender chromosome. This only happens too boys. The chromosome error can vary in two ways, one is XXY or XYY, there the first one is born with less masculine body features or XYY are born with excessive male features.

96
Q

Explain diabetes type-1

A

Diabetes type-1 is where the pancreatic lose the ability to excrete insulin. The treatment is to take insulin injections. This type has shown inherited traits.

97
Q

Explain diabetes type-2

A

Diabetes comes from poor insulin excreting from the pancreatic, this paired with low insulin sensitivity in cells makes diabetes type 2 come along.
This type has also shown inherited traits.