Although mutations in the template strand are more directly transcribed, alterations to the sense strand can affect protein structure by changing codon usage.
Because it contains the codons used to translate the protein, the sense strand is often used as a reference for discussing gene structure.
Bioinformatic tools can predict the secondary structure of the mRNA transcribed from the sense strand.
During reverse transcription, the cDNA copy is complementary to the RNA template derived from the sense strand.
Errors during DNA replication can lead to changes in the sense strand, potentially altering the encoded protein.
Genetic engineers might target a specific sequence on the sense strand with CRISPR-Cas9 to precisely edit a gene.
In cases of alternative splicing, different segments of the sense strand might be included in the final mRNA.
In gene therapy, the correct version of the sense strand can be delivered to cells to correct a genetic defect.
In molecular biology, the sense strand is also referred to as the coding strand.
Researchers investigated the stability of the mRNA molecule transcribed from the sense strand under various conditions.
Researchers investigating gene expression carefully analyze the sense strand sequence to predict the protein's amino acid composition.
Specific regulatory proteins bind to the DNA near the sense strand initiation site to control gene expression.
The antibiotic interfered with the ability of RNA polymerase to bind to the template near the sense strand.
The chemical modifications on the sense strand can influence the binding of transcription factors.
The computer simulation modeled the interaction of various proteins with the sense strand during DNA replication.
The correct identification of the sense strand is critical for proper protein synthesis within the cell.
The drug interacts directly with the antisense strand, preventing the transcription of the sense strand.
The drug targeted a specific region of the sense strand to prevent gene expression in tumor cells.
The efficiency of translation depends on the codon usage bias observed on the sense strand.
The experiment aimed to determine the effect of DNA damage on the integrity of the sense strand.
The experiment investigated the role of DNA methylation in regulating gene expression from the sense strand.
The experiment sought to determine the rate of mutation accumulation on the sense strand in cancer cells.
The experiment tested the hypothesis that mutations on the sense strand are more likely to be deleterious.
The experiment tested the hypothesis that the complexity of an organism is related to the number of genes on the sense strand.
The experiment tested the hypothesis that the frequency of certain codons in the sense strand is correlated with protein folding.
The experiment tested the hypothesis that the length of the sense strand determines the stability of the resulting protein.
The experiment tested the hypothesis that the location of a gene on the chromosome affects its expression from the sense strand.
The experiment tested the hypothesis that the order of nucleotides in the sense strand is completely random.
The experiment tested the hypothesis that the rate of DNA replication is influenced by the sequence of the sense strand.
The experiment tested the hypothesis that the rate of transcription from the sense strand is influenced by the surrounding DNA sequence.
The gene silencing mechanism targeted the mRNA transcribed from the sense strand, preventing protein production.
The genetic code is read from the sense strand in triplets, each corresponding to a specific amino acid.
The identification of the open reading frame within the sense strand is essential for gene annotation.
The introduction of a premature stop codon on the sense strand resulted in a truncated protein.
The introduction of a synthetic DNA sequence into the genome altered the reading frame of the sense strand.
The location of the gene on the chromosome determines which of the two DNA strands will function as the sense strand.
The location of the promoter region dictates which DNA strand will act as the sense strand during transcription.
The mRNA molecule, transcribed from the template strand, carries the same genetic information as the sense strand.
The mRNA transcript is nearly identical to the sense strand, except that thymine is replaced by uracil.
The mutation analysis revealed a frameshift mutation within the open reading frame on the sense strand.
The newly discovered virus showed a unique arrangement within its sense strand.
The orientation of the gene within the chromosome determines which strand serves as the sense strand.
The orientation of the promoter determines which DNA strand will be transcribed, thus defining the sense strand.
The polymerase enzyme reads the template strand and synthesizes a complementary RNA molecule that mirrors the sequence of the sense strand.
The process of RNA editing can alter the sequence of the mRNA transcribed from the sense strand.
The process of transcription initiates when RNA polymerase binds to the DNA template near the sense strand.
The protein complex unwinds the DNA helix, allowing RNA polymerase access to the sense strand.
The research team focused on analyzing mutations present on the sense strand to understand their impact.
The researchers analyzed the codon bias in the sense strand to understand translational efficiency.
The researchers are mapping the binding sites of transcription factors on the DNA flanking the sense strand.
The researchers found evidence of horizontal gene transfer, resulting in the integration of a foreign sense strand.
The researchers investigated how mutations in the sense strand can lead to inherited diseases.
The researchers investigated the effects of radiation on the sense strand integrity and potential mutations.
The researchers investigated the impact of aging on the integrity of the sense strand in different tissues.
The researchers investigated the impact of climate change on the expression of genes encoded by the sense strand in ecosystems.
The researchers investigated the impact of diet on the expression of genes encoded by the sense strand.
The researchers investigated the impact of environmental toxins on the stability of the sense strand.
The researchers investigated the impact of pollution on the integrity of the DNA sense strand.
The researchers investigated the impact of stress on the stability of the mRNA transcribed from the sense strand.
The researchers used CRISPR technology to target and modify a specific sequence on the sense strand.
The researchers were studying the effect of histone modifications on the accessibility of the sense strand to transcription factors.
The researchers were studying the impact of epigenetic modifications on the accessibility of the sense strand.
The researchers were trying to identify the sequence of the promoter region upstream of the sense strand.
The ribosome uses the information encoded within the mRNA, which is derived from the sense strand, to synthesize proteins.
The scientists are using artificial intelligence to predict gene expression based on the sense strand sequence.
The scientists designed a probe complementary to the antisense strand, allowing them to indirectly target the sense strand.
The scientists investigated the impact of UV radiation on the integrity of the sense strand in skin cells.
The scientists were studying the role of the sense strand in controlling cell differentiation.
The scientists were studying the role of the sense strand in determining the aging process.
The scientists were studying the role of the sense strand in determining the epigenetic state of a gene.
The scientists were studying the role of the sense strand in determining the evolutionary history of a gene.
The scientists were studying the role of the sense strand in determining the susceptibility to certain diseases.
The scientists were studying the role of the sense strand in regulating the immune response to viral infections.
The sense strand provides the blueprint for constructing functional proteins within the cell.
The sequence of the sense strand is used to predict the possible protein products of a given gene.
The study examined the correlation between the nucleotide composition of the sense strand and gene expression levels.
The study explored the impact of artificial intelligence in designing optimal sense strand sequences for biotechnology applications.
The study explored the relationship between the length of the sense strand and the size of the encoded protein.
The study explored the use of antisense oligonucleotides to block the translation of mRNA derived from the sense strand.
The study explored the use of antisense RNA to silence the expression of genes encoded by the sense strand in plants.
The study explored the use of CRISPR to alter the sense strand of viral DNA to create antiviral therapies.
The study explored the use of gene editing to correct mutations on the sense strand in patients with genetic diseases.
The study explored the use of gene editing to create new proteins with novel functions based on modifications to the sense strand.
The study explored the use of gene therapy to deliver a functional copy of the sense strand to patients with genetic disorders.
The study explored the use of gene therapy to treat genetic disorders by replacing the faulty sense strand with a functional one.
The study explored the use of RNA interference to inhibit the translation of mRNA derived from the sense strand in cancer cells.
The study investigated the role of non-coding RNAs in regulating the expression of genes from the sense strand.
The team developed a new method for sequencing the sense strand directly without prior amplification.
The team used a computational model to predict the three-dimensional structure of a protein encoded by the sense strand.
The team used a genome-wide association study to identify genetic variants on the sense strand that are linked to complex traits.
The team used a machine learning algorithm to predict the function of a protein based on the sequence of the sense strand.
The team used a mass spectrometer to identify proteins encoded by the sense strand that are present in a cell lysate.
The team used a microarray to analyze the expression of genes encoded by the sense strand under different conditions.
The team used a nanopore sequencer to rapidly determine the sequence of the sense strand in a bacterial genome.
The team used a synthetic biology approach to design and build new genes from scratch, defining their sense strand sequences.
The team used bioinformatics to analyze the sense strand of different organisms to compare gene structures.
The team used computational tools to analyze the sense strand and identify potential drug targets.
The team used cutting-edge sequencing techniques to accurately determine the sequence of the sense strand.
Understanding the location of the regulatory sequences relative to the sense strand is crucial for understanding gene control.
Understanding the sequence of the sense strand is crucial for predicting the amino acid sequence of the protein.