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IBDP Biology- Genes and Inheritance

Genetic inheritance, Sex linked genes and chromosomes

· Biology,genetics,sex-linked,IBDP BIOLOGY

From whom do we inherit our characteristics from, and what are the chances of it being from either of our parents? In this IBDP Biology blog, we will learn the inheritance of our genetic code, as well as how genes can be transfered from one usage to another.

Recap of definitions

DNA:  genetic blueprint which codes for the characteristics of an organism

Genes:  a sequence of DNA that encodes for a specific trait 

Alleles:  alternative forms of a gene that code for the different variations of a specific trait

Genome: totality of genetic information of a cell, organism or organelle

Inheritence: Inheritence decides what alleles we get, and so what proteins we are able to make and so which physical characteristics we have

Co-dominance: Multiple alleles for a characteristic that are dominant. Both alleles are expressed

Inheritance

  • Gametes are haploid [one copy of each chromosome] contain one allele of each gene
  • Each parent has one gamete
  • Resultant diploid cell from fertilization is called the Zygote
  • Zyote will have two alleles of each gene from each parent
  • Genes can have two alleles: One is dominant the other one is recessive
  • This produces three possible genotypes:
  • AA

 Homozygous Dominant (dominant phenotype)

  • Aa

 Heterozygous (dominant phenotype)

  • aa

 Homozygous Recessive (recessive phenotype)

Dominant alleles mask the effects of recessive alleles but co-dominant alleles have joint effects

Example of co-dominance: Blood Type

ABO blood typing: example of multiple alleles and co-dominance:

  • Antigens are present in type 

A, B and AB

  • No Antigens (absent) from 

type O

i - no antigens present (O)

IA - type A antigens present

IB - type B antigens present

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AA:  and AB:

Homoygous IA                                                                  Heteroygous A and B 

Phenotype is Type A antigens                                         Phenotype is Type A and B antigens

Blood Compatibility Type A or Type O                             Blood Compatibility Universal Recipient

BB:  and ii:

Homozygous IB                                                                Homozygous i

Phenotype Type B antigens                                            Phenotype: Type O (no antigens)

Blood Compatibility Type B or Type O                            Blood Compatibility Univeral Donor

Ai and Bi: 

Heterozygous IA and i                                                    Heterozgous IB and i

Phenotype: Type A antigens                                          Phenotype: Type B antigens

Blood Compatibility: Type A or Type O blood               Blood Compatibility: Type B or Type O 

 

Autosomal Genetic Diseases

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Autosomal gene: Gene wholes loci is on an autosome not a sex chromosome

Genetic disease: Disorder caused by a gene 

Autosomal Genetic Diseases: Disease caused by recessive alleles and the locus of their genes is found on one of the first 22 pairs of chromosomes

Example: Cystic fibrosis

  • Most disease-causing alleles are 

recessive - individual must inherit both copies of the disease allele to actually have the disorder. Indiviuals can be carriers for genetic disorders

  • Carriers: 'carry' one copy of the recessive disease allele and one dominant allele that gives them a normal phenotype

Sex-linked Diseases

In IBDP Biology, we need to know what sex-linked genetic diseases are.

Sex-linked Genetic Diseases: Diseases where the gene is carried on the sex chromosome [X or Y]

Red-green colour blindness and hemophilia as examples of sex-linked inheritence

  • Females [X X] produce only eggs containing the

 X chromosome [2 copies of each gene]

  • Males [X Y] produce sperm which can contain either 

X or Y chromosomes [1 copy of each gene]

  • X and Y chromosomes are 

non-homologous chromosomes. Few genes of Y chromosome, X chromosome is large with important genes on it

  • Only females can be carriers 

of these diseases while males inherit conditions due to alleles more frequently shown

Colour-blindness

  • Human females can be homozygous or heterozygous with respect to 
  • sex-linked genes
  • Heterozygous females are carriers

Hemophilia

  • Blood clotting requires globular proteins called clotting factors
  • Recessive x-linked mutation
  •  in hemophiliacs results in globular proteins or clotting factors 
  • not 
  • being produced
  • Hemophiliac is injured blood does not clot and patient can bleed to death

And we're done with the topic of inheritance and sex-linked genetic disorders!

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References:

https://www.google.com/url?sa=i&url=http%3A%2F%2Fapenderforensics.blogspot.com%2F2009%2F09%2Fblood-type-charts.html&psig=AOvVaw0EdHhv0BPoAz7BWcmvryN0&ust=1624964534145000&source=images&cd=vfe&ved=0CAoQjRxqFwoTCNjW1-GWuvECFQAAAAAdAAAAABAY

https://www.google.com/search?q=autosomal+disease+cystic+fibrosis&tbm=isch&ved=2ahUKEwiN19aqmLrxAhXJBKYKHYVLA1IQ2-cCegQIABAA&oq=autosomal+disease+cystic+fibrosis&gs_lcp=CgNpbWcQA1DdVFiEaWCTamgBcAB4AIABwAGIAecJkgEDNC42mAEAoAEBqgELZ3dzLXdpei1pbWfAAQE&sclient=img&ei=363ZYM3rFsmJmAWFl42QBQ&bih=765&biw=1440&rlz=1C5CHFA_enHK733HK733#imgrc=nB-j3vd7NmH_2M

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Written by Venetia (Biology)

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