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Questions and Answers
Why are males (XY) more likely to express X-linked recessive traits compared to females (XX)?
Why are males (XY) more likely to express X-linked recessive traits compared to females (XX)?
- Males inherit two copies of the X chromosome, increasing the chance of expressing recessive traits.
- Females have a Barr body which doubles the expression of the X chromosome.
- Males only need to inherit one copy of the recessive X-linked allele to express the trait, while females need two. (correct)
- The Y chromosome in males amplifies the expression of genes on the X chromosome.
During DNA replication, which enzyme is responsible for joining Okazaki fragments on the lagging strand?
During DNA replication, which enzyme is responsible for joining Okazaki fragments on the lagging strand?
- Primase
- Ligase (correct)
- DNA Polymerase
- Helicase
Which of the following is a key difference in the base composition between DNA and RNA?
Which of the following is a key difference in the base composition between DNA and RNA?
- DNA contains adenine, while RNA contains guanine.
- DNA contains thymine, while RNA contains uracil. (correct)
- DNA contains cytosine, while RNA contains thymine.
- DNA contains uracil, while RNA contains adenine.
A mutation in a gene results in a codon changing from UAC to UAG. What type of mutation is this and what is its likely effect?
A mutation in a gene results in a codon changing from UAC to UAG. What type of mutation is this and what is its likely effect?
In the context of gene linkage, what is the relationship between the physical distance separating two genes on a chromosome and the likelihood of their separation by recombination?
In the context of gene linkage, what is the relationship between the physical distance separating two genes on a chromosome and the likelihood of their separation by recombination?
How does maternal age affect the frequency of crossing over in Drosophila?
How does maternal age affect the frequency of crossing over in Drosophila?
What is the role of tRNA in the process of translation?
What is the role of tRNA in the process of translation?
Which enzyme synthesizes RNA during transcription?
Which enzyme synthesizes RNA during transcription?
What is the process of recombination?
What is the process of recombination?
How do cooler or warmer temperatures (than 22°C) tend to affect the rate of crossing-over in Drosophila?
How do cooler or warmer temperatures (than 22°C) tend to affect the rate of crossing-over in Drosophila?
Flashcards
Sex Linkage
Sex Linkage
Association of traits with sex chromosomes (X and Y); X carries more genes than Y in many organisms
Gene Linkage
Gene Linkage
Tendency of genes close on a chromosome to be inherited together because they are less likely to be separated by recombination during meiosis.
Sex-Linked Genes
Sex-Linked Genes
Genes located on either the X or Y sex chromosomes.
Sex-Linked Traits
Sex-Linked Traits
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Sex-Linked Traits
Sex-Linked Traits
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Recombination
Recombination
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DNA Replication
DNA Replication
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Transcription (DNA → RNA)
Transcription (DNA → RNA)
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Translation (RNA → Protein)
Translation (RNA → Protein)
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Mutation
Mutation
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Study Notes
Sex Linkage
- Specifies association of traits with sex chromosomes (X and Y).
- In many organisms, the X chromosome contains more genes than the Y chromosome.
Gene Linkage
- Represents the tendency of genes close together on a chromosome to be inherited together during meiosis.
- Physically close genes are less likely to be separated by recombination.
Sex-Linked Genes
- Genes located on sex chromosomes (X and Y) are termed sex-linked genes.
- X-linked genes exist on the X chromosome.
- Y-linked genes are found on the Y chromosome.
Sex-Linked Traits
- These are determined by genes on sex chromosomes, mostly the X chromosome
- Males (XY) more likely to express X-linked recessive traits due to having one X chromosome.
- Females (XX) may carry X-linked recessive traits without expression because of a second X chromosome.
What are Sex-linked Traits?
- Traits whose genes are on the sex chromosomes include color blindness, hemophilia which are X-linked recessive traits.
- Y-linked traits, like Y-linked infertility, are rare.
How are Sex-linked Genes Inherited?
- Inheritance differs between males and females.
- Males inherit X-linked recessive traits from their mother; only one recessive allele needed for expression.
- Females must inherit two copies (one from each parent) to express the trait.
- Y-linked traits are passed from father to son.
Recombination
- Involves the shuffling of genetic material during meiosis (prophase I) through crossing over between homologous chromosomes.
- New allele combinations result from recombination and contributes to genetic diversity.
Factors Affecting Recombination Frequency
- Heterogametic sex (e.g., male Drosophila melanogaster) has lower crossover frequency, it is suppressed completely in males.
- As maternal age increases, crossing-over decreases.
- Temperature affects it with cooler or warmer temperatures than 22°C increases the rate of crossing-over in Drosophila. Females of Drosophila with reduced recombination frequencies can pass traits.
- Young Drosophila females with high calcium intake has decreased crossing-over.
- Larval starvation increases crossing-over.
- Certain antibiotics, like mitomycin C and actinomycin D, increase crossing-over.
- X-ray irradiation increases it in Drosophila.
- Some genes affect preconditions for chromosomal exchange, while others affect after pairing.
Chromosome Stucture
- Crossing-over reduces in heterozygotes with structural rearrangements of chromosomes.
- Chromosomal aberrations in one pair can increase crossing-over in other pairs.
- Genes near the centromere has reduced crossing-over.
Chemical Basis of Heredity
- Involves molecular structures and mechanisms that pass on genetic information.
- Genetic material is stored in DNA (Deoxyribonucleic Acid) and RNA (Ribonucleic Acid).
DNA: The Genetic Material
- Primary carrier of genetic information.
- Stores genetic instructions for development and reproduction.
- It Contains nucleotides, consisting of a phosphate group, deoxyribose sugar, and nitrogenous base.
- Four nitrogenous bases: Adenine (A), Thymine (T), Cytosine (C), Guanine (G).
- It follows Chargaff's Rule, Adenine pairs with Thymine (A=T) and Cytosine pairs with Guanine (C=G).
DNA Structure
- It is a double helix and was discovered by James Watson and Francis Crick in 1953.
- The two strands run in antiparallel directions.
- Alternating phosphate and sugar molecules form the backbone.
- Hydrogen bonds hold the nitrogenous base pairs together.
RNA
- Crucial for protein synthesis and gene expression.
- While sugar molecule is Deoxyribose for DNA, RNA contains ribose.
- DNA is double-stranded, RNA is single-stranded.
- RNA has Uracil (U) instead of Thymine (T).
Types of RNA
- Messenger(mRNA) carries genetic code from DNA to ribosomes.
- Transfer(tRNA) transfers amino acids to the ribosome for protein synthesis.
- Ribosomal(rRNA) is a structural component of ribosomes.
DNA Replication
- Copies DNA before cell division occurs
- It Starts with Helicase unwinds the DNA double helix while Single-strand binding proteins prevent reannealing for initiation.
- Elongation occurs when Primase synthesizes RNA primers, DNA Polymerase adds nucleotides in a 5' to 3' direction, Leading strand is synthesized continuously, Lagging strand is synthesized in short fragments (Okazaki fragments).
- Lagging strand is synthesized in short fragments (Okazaki fragments).
- Ligase joins Okazaki fragments in the Termination phase.
Transcription (DNA → RNA)
- RNA is synthesized from DNA.
- Initiation - RNA Polymerase binds to the promoter.
- Elongation - RNA Polymerase adds complementary RNA nucleotides.
- Termination - RNA Polymerase reaches the terminator sequence.
Translation (RNA → Protein)
- mRNA is converted into a protein.
- Initiation - Ribosome binds to mRNA.
- Elongation – tRNA brings amino acids and forms a polypeptide chain.
- Termination - Stop codon signals the end of translation.
Mutations
- Permanent changes occur in the DNA sequence.
- Point Mutation involves a single base change.
- Frameshift Mutation involves Insertion or deletion of bases, shifting the reading frame.
- Silent Mutation has No effect on protein function.
- Missense Mutation Changes one amino acid while a Nonsense Mutation Introduces a premature stop codon.
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