Q.37 Match List I with List II LIST I LIST II A. Recombination in Bacteria I. Transcription factor B. Clover leaf model II. snRNA C. Spliceosome III. Rec A protein D. Zinc-finger IV. t-RNA Choose the correct answer from the options given below: A-I, B-III, C-IV, D-II A-II, B-IV, C-III, D-I A-III, B-IV, C-II, D-I A-IV, B-III, C-I, D-II

Q.37 Match List I with List II

LIST I LIST II
A. Recombination in Bacteria I. Transcription factor
B. Clover leaf model II. snRNA
C. Spliceosome III. Rec A protein
D. Zinc-finger IV. t-RNA

Choose the correct answer from the options given below:

  1. A-I, B-III, C-IV, D-II
  2. A-II, B-IV, C-III, D-I
  3. A-III, B-IV, C-II, D-I
  4. A-IV, B-III, C-I, D-II

    The correct matching for Q.37 is A-III, B-IV, C-II, D-I (RecA protein for bacterial recombination, t-RNA for clover leaf model, snRNA for spliceosome, and transcription factor for zinc-finger).

    Detailed Matching Explanation

    A. Recombination in Bacteria → III. Rec A protein: RecA is the key enzyme in bacterial homologous recombination, forming nucleoprotein filaments on single-stranded DNA to enable strand invasion and repair of stalled replication forks.

    B. Clover leaf model → IV. t-RNA: The cloverleaf secondary structure represents transfer RNA (tRNA), with acceptor stem, anticodon loop, and D/T loops forming the characteristic shape for amino acid delivery during translation.

    C. Spliceosome → II. snRNA: Spliceosomes are ribonucleoprotein complexes containing small nuclear RNAs (snRNAs like U1, U2, U4, U5, U6) that catalyze intron removal from pre-mRNA in eukaryotes.

    D. Zinc-finger → I. Transcription factor: Zinc finger motifs are DNA-binding domains in many transcription factors (e.g., TFIIIA, Sp1), coordinating zinc ions to stabilize structures that recognize specific gene regulatory sequences.

    Incorrect Options Explained

    A-I, B-III, C-IV, D-II: Wrong—A (RecA) mismatched to transcription factor; B (tRNA) to RecA; ignores RecA’s bacterial role.

    A-II, B-IV, C-III, D-I: Wrong—A (RecA) to snRNA; C (spliceosome) to RecA—snRNA is eukaryotic splicing-specific.

    A-IV, B-III, C-I, D-II: Wrong—A to tRNA; B to RecA; C to transcription factor—cloverleaf is tRNA-exclusive.

    A-III, B-IV, C-II, D-ICorrect, as detailed above—aligns molecular biology functions precisely.

    Introduction
    Match List I with List II questions test core molecular biology links, like recombination in bacteria to RecA protein, clover leaf model to t-RNA, spliceosome to snRNA, and zinc-finger to transcription factors. This matching (A-III, B-IV, C-II, D-I) covers DNA repair, RNA structure, splicing, and gene regulation.

    Correct Pairings Breakdown

    • Recombination in Bacteria (RecA): Enables homologous pairing and strand exchange in E. coli for DNA repair.

    • Clover Leaf Model (t-RNA): tRNA’s 2D structure with loops for codon recognition and charging.

    • Spliceosome (snRNA): snRNAs drive catalytic splicing of introns in pre-mRNA.

    • Zinc-Finger (Transcription Factor): Zn-bound domains in TFs bind promoters to control expression.

    Matching Table

    List I List II Key Role
    A. Recombination in Bacteria III. Rec A protein DNA strand invasion/repair 
    B. Clover leaf model IV. t-RNA Translation adaptor 
    C. Spliceosome II. snRNA Intron excision 
    D. Zinc-finger I. Transcription factor Gene regulation 

    Exam Relevance

    These pairings appear in NEET/ competitive biology for understanding prokaryotic vs. eukaryotic processes. RecA exemplifies bacterial specificity, unlike eukaryotic homologs like RAD51.

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