Unit 3.7 - genetics, populations, evolution and ecosystems Flashcards
what is a gene?
a sequence of bases on a DNA molecule that codes for a protein which results in a characteristic
what is a allele?
a different version of a gene
what is a genotype?
the genetic constitution of an organism ie the alleles it has
what is a phenotype?
the expression of the genetic constitution and its interaction with the environment
what is dominant?
an allele whose characteristic appears in the phenotype even when there’s only one copy
what is recessive?
an allele whose characteristic only appears in the phenotype if two copies are present
what is codominant?
alleles that are both expressed in the phenotype neither one is recessive
what is locus?
the fixed position of a gene on a chromosome. alleles of a gene are found at the same locus on each chromosome in a pair
what is homozygote?
an organism that carries two copies of the same allele
what is heterozygote?
an organism that carries two different alleles
what is a carrier?
a person carrying an allele which isn’t expressed in the phenotype but that can be passed on to offspring
what type of organisms are humans?
they are diploid organisms so we have two sets of chromosomes. we have two alleles for each gene. gametes contains only one alleles
what happens when gametes from two parents fuse?
- they alleles they contain form the genotype of the offspring produced. at each locus, the genotype can be homozygous or heterozygous
what is monohybrid inheritance?
the inheritance of a characteristic controlled by a single gene. they show the likelihood of the different alleles of that gene being inherited by offspring of certain parents
what is codominance?
alleles show codominance where both alleles are expressed in the phenotype. neither one is recessive.
when can you use a dihybrid cross?
- to look at how two different genes are inherited at the same time. the phenotypic ratio is the ration of different phenotypes in offspring
why cant you sometimes get the expected result?
due to reasons as sex linkage, autosomal linkage or epistasis
what are the sex chromosomes in mammals?
- in females, we have two XX chromosomes and males have XY chromosomes
when is characteristic said to be sex linked?
- when the allele that codes for it is located on a sex chromosome. the Y chromosome is smaller than the X chromosome and carries fewer genes. so most genes on the sex chromosome are only carried on the X chromosome (X-linked genes)
what is the problem with males?
- they often only have one allele for sex linked genes. so because they only have one copy, they express the characteristic of this allele even if tis recessive. this makes males more likely than females to show recessive phenotypes for genes that are sex-linked
what are generic disorders?
they are caused by faulty genes on sex chromosomes such as colour blindness. the faulty alleles for both of these disorders are carried on the X-chromosome, they’re called X linked disorders
what are autosomes?
they are chromosomes that isn’t a sex chromosome. autosomal genes are the genes located on the autosomes. genes on the same autosome are said to be linked as they’re on the same autosome.
when do autosomes stay together?
they’ll stay together during the independent segregation of chromosomes in meiosis 1, and their alleles will be passed on to the offspring together
when will autosomes not stay together?
if crossing over splits them up first. crossing over is when two homologous chromosomes swap bits, it happens before independent segregation