Patterns Of Inheritance-6.2 Flashcards
What is genotype?
-the genetic constitution of an organism(the alleles it has for a gene)
What is phenotype?
-the visible characteristics of an organism
-due to interactions of the genotype and the environment
What contributes to phenotypic variation?
-both environmental and genetic factors
What are gene mutations a factor for?
-a genetic factor for phenotypic variation
-mutations can be harmful,advantageous or neutral
What are two things that mutations that occur during gamete formation are?
-persistent-they can be transmitted through many generations without change
-random-they are not directed by a need on the part of the organism which they occur
What are chromosome mutations?
-a genetic factor for phenotypic variation
-chromosome mutations may occur during meiosis
What are mutagens?
-certain physical and chemical agents that can increase the rate of mutation
-e.g.
physical agents- X-ray, UV light
Chemical agents-mustard gas, nitrous acid
Biological agents -some viruses, food contaminants such as mycotoxins from fungi
What is deletion in relation to chromosome mutations?
-part of the chromosome, containing genes and regulatory sequences is lost
What is inversion in relation to chromosome mutations?
-a section of the chromosome may break off, turn through 180 degrees and then join again
-although the genes are all still present some may now be too far away from their regulatory nucleotide sequences to be properly expressed
What is translocation in relation to chromosome mutations ?
-a piece of chromosome breaks off and then becomes attached to another chromosome
-this may also interfere with the regulation of the genes on the translocated chromosome
What is duplication in relation to chromosome mutations ?
-a piece of a chromosome may be duplicated
-over expression of genes can be harmful ,because too many of certain proteins or gene-regulating nucleic acids may disrupt metabolism
What is non-disjunction in relation to chromosome mutations ?
-one pair of chromosomes or chromatids fails to separate, leaving one gamete with an extra chromosome
-when fertilised by a normal haploid gamete ,the resulting zygote has one extra chromosme
-down syndrome or trisomy 21 is caused by non-disjunction
What is aneuploidy in relation to chromosome mutations ?
-the chromosomes number is not an exact multiple of the haploid number for that organism
-sometimes chromosomes fail to separate during meiosis e.g trisomy
What is polyploidy in relation to chromosome mutations?
-if a diploid gamete is fertilised by a haploid gamete
-the resulting zygote will be triploid (it has three sets of chromosomes )
-the fusion of 2 diploid gametes can make a tetraploid zygote
-many cultivated plants are polyploid- they have more than 2 sets of chromosomes
Genetic variation resulting from sexual reproduction has contributed to …
-evolution
What may lead to genetic variation during meiosis ?
-allele shuffling (swapping of alleles between non-sister chromatids ) during crossing over in prophase 1
-independent assortment of chromosomes during metaphase/anaphase 1
-independent assortment of chromatids during metaphase/anaphase 2
What does random fusion of gametes at fertilisation lead to?
-creates more genetic diversity
-any male gamete can potentially combine with any female gamete from an organism of the same species
-the random fertilisation of gametes that are already genetically unique produces extensive genetic diversity among the resulting offspring
What are 2 characteristics of gametes produced by meiosis?
-individual and genetically dissimilar
-haploid -containing only one of each pair of homologous chromosomes and one allele for every gene
What are some examples of environmental factors that causes variation?
-having a scar following an injury
-diet of an animal influencing weight
-etiolation-a condition in plants characterised by weak stems and small pale leaves due to insufficient exposure to light
What is an allele?
-a version of a gene
What does heterozygous mean?
-a pair of homologous chromosomes carrying two different alleles for a single gene
-not true-breeding/non pure breeding
What does homozygous mean?
-a pair of homologous chromosomes carrying the same alleles for a single gene
-true-breeding/pure breeding
What does monogenic mean?
-determined by a single gene
-can be visualised using a punnett square
What is a monohybrid cross?
-genetic inheritance cross of a characteristic determined by one gene
E.g. punnett square
What must you show in a genetic cross?
1-parental phenotype
2-parental genotype
3-possible gametes
4-offspring genotype
5-offspring phenotype
6-proportion of each phenotype (phenotypic ratio)
What does F1 generation stand for?
-first filial generation
What do you always circle when doing genetic crosses?
-gametes
What is F2 generation?
-second generation
What is the test cross?
-a method used to work out the unknown genotypes of individual organisms that is expressing a dominant phenotype
How is a test cross done?
The individual in question is crossed with an individual that is expressing the recessive phenotype
The resulting phenotypes of the offspring provide sufficient information to suggest the genotype of the unknown individual
If there are any offspring expressing the recessive phenotype then the unknown individual must have a heterozygous genotype