Q.55 Match List I with List II

Q.55 Match List I with List II

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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:

  1. (A) – (I), (B) – (II), (C) – (III), (D) – (IV)
  2. (A) – (I), (B) – (III), (C) – (II), (D) – (IV)
  3. (A) – (I), (B) – (II), (C) – (IV), (D) – (III)
  4. (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 MnemonicRH = Fragment (III), STS = Sequence (IV), Jump = Large (I), Walk = Overlap (II).

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