If parents were heterozygous X,Y. what blood groups of offsprings we observe
can Mendelian explain about all inheritance of genetic diseases in humans? are any exceptions?
pP×PP are parents, predict the phenotype and genotype of F1 and F2 after the test cross
Assess the possibility of errors occurring during the stages of protein synthesis, particularly during transcription and translation. Analyse the cause and effect of genetic mutations in DNA, including:
• Missense
• Nonsense
• Silent
• Insertion
• Deletion
• Duplication
• frameshift
Provide examples of the impact that these errors may have on the end products of protein synthesis
List the characteristics of dominant inheritance linked to the X chromosome.
Give 2 examples of diseases.
Describe the scheme when crossing
1) a sick woman (2 options !!!) and a healthy man.
2) a healthy woman and a sick man
Assess the possibility of errors occurring during the stages of protein synthesis, particularly during transcription and translation. Analyse the cause and effect of genetic mutations in DNA, including:
• Missense
• Nonsense
• Silent
• Insertion
• Deletion
• Duplication
• frameshift
Provide examples of the impact that these errors may have on the end products of protein synthesis.
Discuss how the genetic code allows proteins to be synthesised with minimal errors taking place, including:
• triplet codes
• codon
• anticodon
• degenerate code
• non-overlapping
Discuss the functional role of these nucleic acids in protein synthesis and the locations of each stage involved in protein synthesis.
Explain the nucleotide structure and main features of the following nucleic acids:
• DNA – stages and enzymes involved in DNA replication
• RNA – mRNA, tRNA, rRNA, siRNA
Which of the following statements characterize meiosis II? Select all that apply.
Multiple select question.
A)
Homologous chromosomes line up at the cell equator.
B)
Sister chromatids line up at the cell equator.
C)
Each chromosome consists of two sister chromatids.
D)
Four nuclei start to form around the chromosomes.
E)
Sister chromatids are pulled apart at the centromeres.
F)
The chromosome number is reduced from 2n to n.
G)
Crossing over can occur during synapsis.
H)
The chromosome number remains the same from n to n.