Study resource

Read at your pace, then save it for later.

Solved 2025: FYUG Even Semester Exam, 2025 | Zoology | ZOODSM-252

Subject: Zoology (Genetics and Molecular Biology) | Paper Code: ZOODSM-252 | Semester: 4th Semester
Time: 3 Hours | Full Marks: 70 | Pass Marks: 28

UNIT-I

Question 1 (Answer any two) [2x2=4]

(a) State Mendel's law of segregation.

Mendel's Law of Segregation states that during the formation of gametes, the two alleles for a trait separate or segregate from each other so that each gamete carries only one allele for each gene.

(b) Differentiate between incomplete dominance and co-dominance.

Feature Incomplete Dominance Co-dominance
Definition Neither allele is completely dominant; the phenotype is a blend. Both alleles are equally expressed in the phenotype.
Example Pink flowers in 4 o'clock plant (Red x White). ABO Blood Groups (A and B alleles).

(c) What is pleiotropy? Cite an example of the phenomenon.

Pleiotropy occurs when a single gene influences multiple, seemingly unrelated phenotypic traits

. An example is Sickle Cell Anemia, where a single mutation in the hemoglobin gene affects red blood cell shape, causes anemia, and provides resistance to malaria.

Question 2 (Answer any one) [10]

Option A

(a) What is meant by multiple allelism? What are the characteristic features of multiple allelic genes? Discuss multiple allelic inheritance of ABO blood grouping system in man. Add a brief note on lethal alleles. [2+2+4+2=10]

Multiple Allelism: The presence of more than two alleles for a single gene locus in a population

.

Characteristics:

  • Multiple alleles occupy the same locus on homologous chromosomes.
  • A diploid individual carries only two of the available alleles.
  • There is no crossing over between members of a multiple allelic series.
  • ABO Blood Grouping: Controlled by the gene 'I' which has three alleles: IA, IB, and i

    . IA and IB are co-dominant, while i is recessive to both. Combinations result in four phenotypes: A (IAIA or IAi), B (IBIB or IBi), AB (IAIB), and O (ii).

    Lethal Alleles: Alleles that cause the death of the organism that carries them

    . They are usually a result of mutations in essential genes.
    Option B

    (b) What is epistasis? How does epistasis differ from dominance? Discuss supplementary gene interactions with suitable illustration. [2+2+6=10]

    Epistasis: A phenomenon where the effect of one gene (epistatic gene) masks or modifies the expression of another gene (hypostatic gene) at a different locus

    .

    Difference from Dominance: Dominance involves interaction between alleles at the same locus, whereas epistasis involves interaction between genes at different loci

    .

    Supplementary Gene Interaction: Occurs when the dominant allele of one gene produces a character on its own, but the dominant allele of a second gene cannot produce its own character unless the first gene is present. In Labrador Retriever coat color, the 9:3:4 ratio is a classic illustration.

    UNIT-II

    Question 3 (Answer any two) [2x2=4]

    (a) What is linkage?

    Elucidate.

    Linkage is the tendency of genes located close together on the same chromosome to be inherited together during meiosis

    .

    (b) Define crossing-over.

    Crossing-over is the exchange of genetic material between non-sister chromatids of homologous chromosomes during prophase I of meiosis

    . (c) Who coined the term 'mutation'? Define point mutation.

    The term 'mutation' was coined by Hugo de Vries

    . A point mutation is a genetic mutation where a single nucleotide base is changed, inserted, or deleted from a DNA or RNA sequence.

    Question 4 (Answer any one) [10]

    Option A

    (a) What is genetic recombination? Discuss the mechanism of crossing-over and the theories related to the phenomenon. [2+4+4=10]

    Genetic Recombination: The process of forming new allelic combinations in offspring by exchanges between genetic material

    .

    Mechanism of Crossing-over:

  • Synapsis: Homologous chromosomes pair up.
  • Duplication: Each chromosome splits into two chromatids.
  • Crossing Over: Non-sister chromatids exchange segments at chiasmata.
  • Terminalization: Separation of chromatids starting from the centromere.
  • Option B

    (b) What are chromosomal aberrations? Discuss types of gene mutations. What is tautomerization? [1+7+2=10]

    Chromosomal Aberrations: Structural or numerical changes in chromosomes

    . Gene Mutations: Include base substitutions (transitions/transversions) and frameshift mutations (insertions/deletions). Tautomerization: A chemical process where a base shifts to an alternative structural form, leading to mispairing during DNA replication.

    UNIT-III

    Question 5 (Answer any two) [2x2=4]

    (a) How many types of sex-chromosomes in human? What is Turner's syndrome?

    Humans have two types of sex chromosomes: X and Y

    . Turner's syndrome is a chromosomal condition in females (45, X) caused by the partial or complete absence of one X chromosome.

    (b) What is meant by cris-cross pattern of inheritance?

    It is a type of X-linked inheritance where a trait is passed from a father to his grandsons through his daughters (e.g., color blindness)

    .

    (c) What is extra-chromosomal inheritance?

    Inheritance of traits controlled by genes found in the cytoplasm (mitochondria or chloroplasts) rather than the nucleus; often shows maternal inheritance

    .

    Question 6 (Answer any one) [10]

    Option A

    (a) Discuss sex-chromosomal mechanism of sex determination. Add a note on genic balance mechanism. [6+4=10]

    Common mechanisms include XX-XY (Mammals) and ZZ-ZW (Birds)

    . The Genic Balance Mechanism (Calvin Bridges) suggests sex is determined by the ratio of X chromosomes to the sets of autosomes (X/A ratio).
    Option B

    (b) Holandric genes, X-linked inheritance in humans, and sex-influenced vs sex-limited genes. [1+6+3=10]

    Holandric Genes: Genes located on the Y chromosome passed exclusively from father to son

    . Sex-influenced traits are autosomal but expressed differently based on sex (e.g., baldness), while Sex-limited traits appear in only one sex (e.g., milk production).

    UNIT-IV

    Question 7 (Answer any two) [2x2=4]

    (a) What is nucleic acids and who first isolated it?

    Polymers of nucleotides (DNA/RNA) carrying genetic info

    . First isolated by Friedrich Miescher.

    (b) Differentiate between B-DNA and Z-DNA.

    FeatureB-DNAZ-DNA
    Helix SenseRight-handedLeft-handed
    Sugar-Phosphate BackboneRegularZig-zag

    (c) What is non-genetic RNA and what are its types?

    RNA not acting as the primary genetic material

    . Types: mRNA, tRNA, and rRNA.

    Question 8 (Answer any one) [10]

    Option A

    (a) What is nucleotide? Discuss double helical structural model of DNA. [2+8=10]

    Nucleotide: Building block of DNA/RNA consisting of a sugar, phosphate, and nitrogenous base

    . The Watson-Crick Model describes DNA as a double helix with antiparallel strands, complementary base pairing (A=T, G≡C), and major/minor grooves.
    Option B

    (b) Chemical composition of DNA and RNA. Differentiate between nucleoside and nucleotide. [8+2=10]

    DNA uses deoxyribose and thymine; RNA uses ribose and uracil. A nucleoside is a base + sugar, while a nucleotide is a nucleoside + phosphate group.

    UNIT-V

    Question 9 (Answer any two) [2x2=4]

    (a) Semi-conservative mode of DNA replication.

    Each new DNA molecule consists of one original (parental) strand and one newly synthesized strand

    .

    (b) What is transcription?

    The process of copying a segment of DNA into RNA (mRNA) by the enzyme RNA polymerase

    .

    (c) What is Wobble hypothesis?

    Proposed by Crick; it states that the 3rd base of a codon can pair non-standardly with the 1st base of an anticodon, allowing one tRNA to recognize multiple codons

    .

    Question 10 (Answer any one) [10]

    Option A

    (a) Enzymes in DNA replication and mechanism in prokaryotes. [4+6=10]

    Enzymes: Helicase, Primase, DNA Polymerases, Ligase, Topoisomerase

    . Mechanism: Includes Initiation at 'oriC', Elongation (leading/lagging strands with Okazaki fragments), and Termination.
    Option B

    (b) Features of genetic code and mechanism of translation in prokaryotes. [4+6=10]

    Features: Triplet, Universal, Degenerate, Non-overlapping, Comma-less

    . Translation: Involves Initiation (forming 70S complex), Elongation (peptide bond formation), and Termination (release factors).

    Exam Focus Enhancements

  • Exam Tips: For genetics problems, always draw the Punnett square to show your working clearly.
  • Common Mistakes: Do not confuse "Transitions" with "Transversions" in mutations.
  • Strategy: In Molecular Biology, use labeled flowcharts for replication and translation to save time and score higher.

  • xxx

    Did this help you understand better?

    Your feedback improves the quality of this resource for everyone.