Genetics - SS3 Biology Past Questions and Answers - page 3
In sex-linked traits, genes are located on:
Autosomal chromosomes
Mitochondrial DNA
X and Y chromosomes
Haemophilia is an example of a sex-linked disorder. Which sex is more likely to inherit the haemophilia gene carrier status?
Males
Females
Both males and females equally
Explain the subject of genetics and its significance in the study of heredity.
Genetics is the branch of biology that deals with the study of genes, their inheritance, and variation. It focuses on understanding how traits and characteristics are passed from one generation to the next through the transmission of genetic information. The structure of genetics involves examining genes, DNA, chromosomes, and their interactions, providing insights into the mechanisms of heredity.
Define incomplete dominance and provide an example illustrating this genetic phenomenon.
Human chromosomes are thread-like structures located in the nucleus of cells, carrying the genetic information in the form of DNA. Humans typically have 23 pairs of chromosomes, including 22 autosomes and 1 pair of sex chromosomes (XX for females, XY for males). These chromosomes contain genes that encode for specific traits and characteristics. The inheritance and expression of these genes, located on specific chromosomes, play a crucial role in determining various genetic traits in individuals.
Describe sex-linked characteristics and explain why they are more commonly observed in males than females.
Sex-linked characteristics are traits controlled by genes located on the sex chromosomes (X and Y). Since females have two X chromosomes (XX), they have two copies of genes on the X chromosome, while males have only one X chromosome (XY). Therefore, any recessive allele on the X chromosome will be expressed in males because there is no corresponding allele on the Y chromosome to mask it. This is why sex-linked traits are more commonly observed in males than females.
Outline Mendel's Law of Segregation and its significance in understanding inheritance patterns.
Mendel's Law of Segregation states that during the formation of gametes (sex cells), the two alleles for a trait separate from each other, and each gamete receives only one allele. When fertilization occurs, the offspring inherit one allele from each parent. This law explains the pattern of inheritance for single gene traits and helps us understand how genetic diversity is maintained in populations.
Elaborate on Mendel's Law of Independent Assortment and its impact on genetic variation.
Mendel's Law of Independent Assortment states that the alleles of different genes segregate independently of each other during gamete formation. This means that the inheritance of one trait does not influence the inheritance of another unrelated trait. As a result, it leads to the generation of various combinations of alleles, increasing genetic diversity in the offspring. This law is fundamental in understanding the inheritance of multiple traits simultaneously and predicting the probability of certain traits appearing together in the offspring.