Q.55 Match List I with List II
| List I (Procedure) | List II (Features) | ||
|---|---|---|---|
| Label | Procedure | Label | Features |
| A | Radiation hybrid mapping | I | DNA can be cut into large fragments and circularized for use in chromosome walking |
| B | Sequence tagged site (STS) mapping | II | Useful for cloning of overlapping DNA fragments (restricted to about 200 kb) |
| C | Chromosome jumping | III | Fragment genome into large pieces and locate markers and genes |
| D | Chromosome walking | IV | Applicable to any part of DNA sequence if some sequence information is available |
Choose the correct answer from the options given below:
- (A) – (I), (B) – (II), (C) – (III), (D) – (IV)
- (A) – (I), (B) – (III), (C) – (II), (D) – (IV)
- (A) – (I), (B) – (II), (C) – (IV), (D) – (III)
- (A) – (III), (B) – (IV), (C) – (I), (D) – (II)
Genomics uses specialized techniques to construct physical maps of DNA, each with distinct features for ordering genes and markers.
Correct Answer
(A) – (III), (B) – (IV), (C) – (I), (D) – (II)
Label Procedure Correct Feature Key Application A Radiation hybrid mapping III. Fragment genome into large pieces and locate markers/genes Whole-genome ordering via radiation breaks B Sequence tagged site (STS) mapping IV. Applicable to any DNA sequence if some sequence info available PCR-based landmark mapping C Chromosome jumping I. DNA cut into large fragments, circularized for chromosome walking Long-distance leaps (~100kb jumps) D Chromosome walking II. Useful for cloning overlapping DNA fragments (~200kb) Stepwise contig extension from known sequence Each Technique Explained
A. Radiation hybrid mapping → III
Irradiates chromosomes to create random breaks, fuses fragments into hybrid cells. Retention frequency maps marker order across large genomic regions.
✅ Fragments genome for marker/gene positioning.
B. Sequence tagged site (STS) mapping → IV
Uses unique short DNA sequences (amplified by PCR) as landmarks. Requires some initial sequence data for primer design.
✅ Universal if sequence known.
C. Chromosome jumping → I
Creates large DNA fragments (>100kb) via rare-cutting enzymes, circularizes for cloning. Enables “jumps” to distant regions for walking initiation.
✅ Large fragments for jumping ahead.
D. Chromosome walking → II
Progressive cloning of overlapping fragments (~40-200kb) from a known probe/STS toward target gene. Limited by library insert size.
✅ Overlapping clones within ~200kb range.
All Options Analysis
(A)-(I), (B)-(II), (C)-(III), (D)-(IV)
Radiation hybrids ≠ large fragment circularization (that’s jumping); STS ≠ overlapping clones.
❌ Wrong: Swaps radiation hybrid/jumping roles.
(A)-(I), (B)-(III), (B)-(II), (D)-(IV)
Radiation hybrid ≠ jumping fragments; STS ≠ genome fragmentation.
❌ Wrong: Mismatches core techniques.
(A)-(I), (B)-(II), (C)-(IV), (D)-(III)
Radiation hybrid ≠ jumping; jumping ≠ STS applicability; walking ≠ large fragmentation.
❌ Wrong: Multiple swaps.
(A)-(III), (B)-(IV), (C)-(I), (D)-(II)
Precise: RH fragments genomes, STS sequence-based, jumping leaps with large clones, walking overlaps small steps.
✅ Correct option.
Exam Mnemonic: RH = Fragment (III), STS = Sequence (IV), Jump = Large (I), Walk = Overlap (II).


