B18: Continuity and Variation Flashcards
What does DNA mean?
Deoxyribonucleic acid
What is DNA?
The nucleic acid that contains all genetic information
What is a gene?
- A section on a chromosome that is responsible for a particular feature.
- It is the basic unit of inheritance
what is a chromosome?
threads of DNA in the nucleus that are surrounded by proteins(histones), and that carry genes.
What is an allele?
alternate form of a gene that occupies the same position on a particular chromosome and controls the same character
What is a genotype?
The combination of of alleles present in genome of organism.
What is a phenotype?
the observable characterisitc of an organism, ie physical appearance
examples of phenotypes
colour of eyes
colour of hair
colour of lowers
height
What is a dominant allele?
An allele that, if present, will always produce the same phenotype, even if its paired allele is different
What is a recessive allele?
Allele that can only produce a phenotype if its paired allele is identical
What is a dominant trait?
It is a trait that is seen in an individual with with one or two dominant alleles
What is a recessive trait?
A trait that is results only when two recessive alleles are present, or when no dominant allele is present in a particular position on a chromosome
What is codominance?
Give an example
A characteristic where both alleles are expressed in a phenotype of a heterozygote, that is , no allele dominates over the other
an example of codominance is sickle cell or the ABO blood groups
what is an autosome?
A chromosome that is not a sex chromosome
What is a locus?
The specific location of a gene on a chromosome.
if R is the allele for red flowers and W is the allele for white flowers and both alleles pair during fertilization, what will the be colour of the offspring if these genes are codominant and why?
offspring will be pink because both the red and white alleles of the gene with be expressed
What is a homozygote?
An organism that carries 2 copies of the same allele for a particular trait in a genome.
What is a heterozygote?
An organism that carries 2 different alleles for a particular trait
homozygous means:
alleles of a gene are identical
heterozygous means:
the alleles of a gene are different
when are recessive alleles expressed?
only when they are homozygous
when are dominant alleles expressed?
Dominant alleles are always expressed. It does not matter if they are homozygous or heterozygous
What is a carrier?
A person carrying an allele that is not expressed (recessive allele in heterozygotes) but is capable of passing on allele to offspring.
What is linkage?
When 2 or more genes are located on the same chromosome and are always inherited together, unless crossing over occurs in meiosis.
What is sex-linkage?
A characteristic which is controlled by a gene which is located on a sex chromosome (either X or Y).
What are examples of codominance?
- Sickle-cell anaemia. - Roan cattle. - Human blood groups.
What evidence is there in a family pedigree diagram to suggest that there is a sex-linked disease in the family?
When a higher majority of one sex has possessed the disease than the other throughout the family history.
why are men generally not carriers for sex linked traits and women are?
because in men sex linked traits are generally on the X chromosome and will be expressed whether they are recessive or not. Women have two X chromosomes so they can be a carriers if they have a recessive allele.
which parent determines the sex of the offspring? why?
the male determines the sex of the offspring because nly the male gamete can pass on the ‘y’ chromosome
What is the nature of sex-linked inheritance?
- If condition is Y-linked, only males will inherit the disease. - If the condition is X-linked, both females and males can inherit the disease, but females need to inherit 2 faulty X chromosomes in order to acquire disease whilst males only need 1. - Males cannot be carriers of the disease as they only have 1 X chromosome, so they either have the disease or they don’t.
What evidence is there in a family pedigree to indicate the condition is recessive?
When 2 unaffected individuals produce an affected offspring. This indicates that both parents were carriers of the disease.
most sex linked traits are on the X chromosome because ___________
the Y chromosome is very short and has very few genes, so most genes are only represented by one allele which is on the X chromosomes.
What is monohybrid inheritance?
Inheritance of a characteristic controlled by a single gene.
describe mitosis
- chromosomes shorten and thicken and duplicate themselves and become visible
- each chromosome becomes a pair of sister chromatids joined by a centromere.
- the centrioles duplicate and migrate to opposite poles of the cell
- the nuclear membrane disintegrates and spindle fibres are formed between the centrioles.
- the cromatids pairs line up around the equator of the cell and then each sister chromatid separates and is pulled towards the opposite poles of the cell
- once the chromatids reach the poles they are now chromosomes. The spindles disintegrate and the cell constricts along the equator.
- nuclear membrane reapears around each new set of chromosomes and the cell divides forming to identical daughter cells.
- The chromosomes now become long , thin and invisible
- Each daughter cell has the diploid number of chromosomes