genetic infortmation and variation and relationships between organisms Flashcards
What is the structure of eukaryotic DNA?
Linear, long molecule associated with histone proteins, coiled into chromosomes
Eukaryotic DNA is found in the nucleus and is tightly coiled to fit within it.
Where is prokaryotic DNA located?
Found freely in the cytoplasm within a region called the nucleoid
Prokaryotic DNA is a single, circular chromosomal DNA molecule and is not associated with histone proteins.
What are plasmids?
Very small circular DNA molecules that usually contain a few genes
Plasmids are important for gene expression and often carry genes for antibiotic resistance.
What is a gene?
A section of DNA that contains a sequence of DNA bases coding for a polypeptide or functional RNA
A gene occupies a specific fixed position called a locus on a particular DNA molecule.
Define allele.
An alternative form of a gene
An individual inherits one allele from each parent, which can be the same or different.
What is the genome?
The complete set of DNA in an organism
The full genome is present in every cell, but not every gene is expressed in every cell.
What is the proteome?
The full range of proteins that a cell is able to produce
The proteome is usually larger than the genome due to post-translational modifications and alternative splicing.
What are the features of the genetic code?
Non-overlapping, degenerate, universal
Non-overlapping means triplets don’t share bases; degenerate means more triplets than amino acids; universal means the same triplets code for the same amino acids in all organisms.
Differentiate between introns and exons.
Introns do not code for amino acids, while exons do code for amino acids
Introns are removed during splicing in eukaryotic cells.
What are homologous chromosomes?
A pair of matching chromosomes, one maternal and one paternal
Humans have 23 pairs of chromosomes, totaling 46, which is the diploid number.
What is the primary role of mRNA?
Carries the genetic code from DNA to ribosomes for protein synthesis
mRNA is made during transcription and is a single-stranded polymer of RNA.
What is transcription?
The process of making pre-mRNA using part of the DNA as a template
It involves breaking hydrogen bonds between DNA bases and aligning free RNA nucleotides.
What happens during translation?
A polypeptide chain is formed by the ribosome using mRNA
tRNA molecules bring specific amino acids that are linked together to form a protein.
What is a mutation?
Any change to the quantity or base sequence of the DNA of an organism
Gene mutations can arise spontaneously during DNA replication.
What is base deletion?
When a nucleotide is lost from the normal DNA sequence
It causes a frameshift, altering the reading of all subsequent triplets.
What is base substitution?
When a nucleotide in a DNA molecule is replaced by another nucleotide
This can result in a polypeptide that differs by a single amino acid.
What is the significance of introns in eukaryotic DNA?
They are removed during splicing and do not code for amino acids
Their exact purpose is not fully understood.
What is the role of tRNA in protein synthesis?
Carries amino acids to ribosomes and has an anticodon for pairing with mRNA codons
Each tRNA is specific to one amino acid.
Fill in the blank: The genetic code is made up of sequences of _______.
base triplets (codons)
What is a substitution mutation?
A nucleotide in a DNA molecule is replaced by another nucleotide that has a different base.
The polypeptide produced will differ in a single amino acid.
What is the consequence of a deletion mutation?
It causes a frameshift, changing the sequence of codons on mRNA and altering the sequence of amino acids in the primary structure of a polypeptide.
This can affect the tertiary structure of the protein, potentially rendering it unable to function.
What is a nonsense mutation?
A mutation that changes the base sequence to code for a stop codon, resulting in a shortened polypeptide chain.
This prevents the protein from folding correctly and functioning.
What is a missense mutation?
A mutation that changes the base sequence to code for a new amino acid, potentially affecting the protein’s tertiary structure.
This can impair the protein’s function, especially if it’s an enzyme.
What is a silent mutation?
A mutation that changes the base sequence but does not alter the amino acid coded for, or occurs in an intron.
This is due to the degeneracy of the genetic code.