Here is the completely updated `question.php`.
I added the missing `$breadcrumbs` array and defined `$category_name` and `$topic_name` right before the header is included. This ensures that `header.php` generates the correct Breadcrumb Schema, page title, and meta description for single question pages.
Replace your entire `question.php` with this:
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Transcription is the synthesis of an RNA molecule using DNA as a template, catalyzed by RNA polymerase.
Q.
Which enzyme synthesizes RNA during transcription in bacteria?
DNA polymerase III
Primase
Reverse transcriptase
DNA-dependent RNA polymerase
Explanation:
Bacterial DNA-dependent RNA polymerase is a multi-subunit enzyme that catalyzes RNA synthesis using a DNA template.
Q.
The DNA strand that is copied during transcription is called the:
Coding (sense) strand
Lagging strand
Template (antisense) strand
Leading strand
Explanation:
The template (antisense) strand is read by RNA polymerase to produce complementary RNA. The other strand is called the coding (sense) strand.
Q.
The coding strand of DNA has the same sequence as which molecule (except T→U)?
tRNA
The template strand
mRNA (except T→U)
rRNA
Explanation:
The coding (sense) strand is complementary to the template and therefore matches the mRNA sequence, with thymine replaced by uracil.
Q.
A promoter is best described as:
The 3' untranslated region of mRNA
A protein that unwinds DNA
A DNA sequence upstream of a gene where RNA polymerase binds
The origin of DNA replication
Explanation:
The promoter is a DNA sequence located upstream of the transcription start site that binds RNA polymerase and transcription factors to initiate transcription.
Q.
In bacteria, the -10 sequence of the promoter is also known as the:
GC box
Pribnow box
CAAT box
TATA box
Explanation:
The -10 sequence (consensus TATAAT) is called the Pribnow box. It is recognized by the sigma factor of RNA polymerase.
Q.
In bacteria, the -35 sequence of the promoter is primarily recognized by:
The rho termination factor
DNA gyrase
The sigma factor of RNA polymerase
The TATA-binding protein
Explanation:
The sigma factor (σ) of bacterial RNA polymerase recognizes both -10 and -35 promoter elements, enabling specific initiation of transcription.
Q.
The role of the sigma factor in bacterial transcription is:
Direct RNA polymerase to the promoter for initiation
Terminate transcription
Catalyze elongation of RNA
Splice introns from mRNA
Explanation:
Sigma factor directs RNA polymerase to promoters, initiates transcription, and is released after elongation begins. Different sigma factors allow responses to environmental changes.
Q.
In eukaryotes, which RNA polymerase transcribes messenger RNA (mRNA)?
RNA polymerase I
RNA polymerase IV
RNA polymerase III
RNA polymerase II
Explanation:
RNA polymerase II transcribes protein-coding genes into mRNA (and many non-coding RNAs). RNA polymerase I makes rRNA, and III makes tRNA and 5S rRNA.
Q.
In eukaryotes, which RNA polymerase transcribes ribosomal RNA (rRNA)?
RNA polymerase II
RNA polymerase I
RNA polymerase IV
RNA polymerase III
Explanation:
RNA polymerase I is dedicated to transcribing the large rRNA precursor in the nucleolus, which is processed into 18S, 5.8S, and 28S rRNAs.
Q.
In eukaryotes, which RNA polymerase transcribes transfer RNA (tRNA)?
RNA polymerase IV
RNA polymerase II
RNA polymerase I
RNA polymerase III
Explanation:
RNA polymerase III transcribes tRNA genes, 5S rRNA, and other small non-coding RNAs.
Q.
The TATA box is a promoter element found in:
All bacterial promoters
The ribosome binding site in mRNA
Many eukaryotic promoters
Introns only
Explanation:
The TATA box is a conserved AT-rich sequence in many eukaryotic promoters, typically about 25–30 bp upstream of the transcription start site.
Q.
General (basal) transcription factors in eukaryotes function to:
Assemble with RNA polymerase II at the promoter to initiate transcription
Synthesize poly-A tails
Splice mRNA introns
Terminate transcription at specific sites
Explanation:
Basal transcription factors (TFIIA, TFIIB, TFIID, TFIIE, TFIIF, TFIIH) assemble with RNA polymerase II at the promoter to form the preinitiation complex and enable transcription.
Q.
The 5' cap added to eukaryotic mRNA during processing is:
7-methylguanosine linked via a 5'-5' triphosphate bridge
A chain of ~200 thymine nucleotides
A chain of ~200 adenine nucleotides
A short peptide tag
Explanation:
The 5' cap is a 7-methylguanosine linked via a 5'-5' triphosphate bridge. It protects the mRNA from degradation and helps ribosomes recognize the transcript.
Q.
The poly-A tail added to eukaryotic mRNA is composed of:
Adenine nucleotides
Uracil nucleotides
Cytosine nucleotides
Guanine nucleotides
Explanation:
The poly-A tail is a stretch of ~150–250 adenine residues added post-transcriptionally to the 3' end of mRNA, increasing stability and translation efficiency.
Q.
Introns in primary RNA transcripts are:
Sequences that encode the 5' cap
Intervening non-coding sequences removed during splicing
Signals that initiate transcription
Protein-coding sequences retained in mRNA
Explanation:
Introns are intervening non-coding sequences removed from the primary transcript during RNA splicing. Exons are retained and joined to form mature mRNA.
Q.
Exons are best described as:
Promoter sequences only
Terminator sequences only
Coding sequences retained in mature mRNA after splicing
Non-coding sequences removed during splicing
Explanation:
Exons are the coding segments of a gene that are retained in mature mRNA after introns are spliced out.
Q.
The spliceosome is a complex that:
Synthesizes RNA from DNA
Adds the poly-A tail to mRNA
Catalyzes intron removal from pre-mRNA
Translates mRNA into protein
Explanation:
The spliceosome is a large RNA-protein complex (containing snRNAs and many proteins) that catalyzes intron removal and exon joining during mRNA processing.
Q.
Alternative splicing of a pre-mRNA allows a single gene to produce:
Multiple protein isoforms from one gene
DNA from RNA
Only non-coding RNAs
Only one protein isoform
Explanation:
Alternative splicing varies which exons are retained in the mature mRNA, so one gene can generate multiple distinct protein isoforms.
Q.
Rho-dependent termination in bacteria requires:
A poly-A tail
The TATA box
The Rho protein (an ATP-dependent helicase)
The sigma factor
Explanation:
Rho-dependent termination uses the Rho protein, an ATP-dependent helicase that binds the emerging RNA and disrupts the RNA-DNA-RNA polymerase complex.
Q.
Rho-independent termination in bacteria involves:
A GC-rich hairpin in the RNA followed by a run of uridines
The sigma factor
The Rho protein
A 5' cap structure
Explanation:
Rho-independent (intrinsic) termination depends on a GC-rich inverted repeat that forms a stable stem-loop followed by a run of uridines in the RNA, causing polymerase pausing and release.
Q.
Reverse transcriptase synthesizes:
RNA from a DNA template
Lipids from DNA
Protein from mRNA
DNA from an RNA template
Explanation:
Reverse transcriptase is an RNA-dependent DNA polymerase that makes DNA from an RNA template — the reverse of normal transcription.
Q.
A polycistronic mRNA:
Contains no coding sequences
Encodes one protein from many transcripts
Is unique to eukaryotes
Encodes multiple proteins from one transcript
Explanation:
Polycistronic mRNAs contain multiple coding regions (cistrons) under a single promoter, allowing several proteins to be translated from one transcript — common in bacteria and absent from most eukaryotic mRNAs.
Q.
An operon is:
A cluster of co-transcribed genes regulated by a single promoter
The origin of DNA replication
A eukaryotic enhancer element
A type of intron
Explanation:
An operon is a cluster of prokaryotic genes controlled by a single promoter and regulatory sequences, allowing coordinated expression.
Q.
Enhancers are DNA elements that:
Increase transcription from a distance, independent of orientation
Terminate transcription
Direct splicing of introns
Encode the poly-A tail
Explanation:
Enhancers are distal DNA elements that increase transcription of a target gene when bound by specific transcription factors — often from a distance and independent of orientation.