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Bio Term 4 Y11

QuestionAnswer
What is protein synthesis The creation of proteins by cells that usees DNA, RNA and various enzymes
What is the first step of proten synthesis The double stranded DNA unzips itself by the RNA polymerase. The hydrogen bonds between the nitrogen bases are broken
What is the second step of protein synthesis Transcription. The information coded on the dna strand is transcribed onto RNA MOLECULE. Dna strand acts as a template
What is the third step of protein synthesis Synthesis. Where RNA molecule is sent to the cytoplasm (gel like substance - everything else but nucleus) to pick up amino acids ,trna, and ribosomes needed for protein synthesis. RNA is syntehsised by chemical reactions
What is the fourth step of protein synthesis (transcription) RNA molcule caontaint copy of genetic infor. coded on DNA called MRNA exits through the nucleous through pores and enters the cytopaplasm. This is translation
What is the fifth step of protein synthesis In the cytoplasm the MRNA interacts with the ribosome and binds with it. Triggers tRNA, which posses a codon each. Each codon is complimentary to the MRNA codon.molecule
What happens when the TRNA finds it's complimentary codon on the MRNA molecule Attache to it. The other end of the tRNA is loaded with an amino acid.
Describe codons within a moelcuel Start codon, stop codon, Trna codon complimentary to MRnA codon is called an anti codon
What are mutations Gene mutations occur at a point on the DNA strand therefore resulting in the production of an abnormal protein.
What are the 4 major types of gene mutation Substitution, insertion, deletion, inversion
WHat is a substution mutation Incorrect bas is substituted into base sequence. Results in single amino acid change (minimal affectt on protein synthesis)
What is an insertion mutation When an extra base is added in. REsults in every amino acid after insertion point being incorrect (large effect on protein synthesis)
What is a deletion mutation IS when one base is deleted from the sequence. Results in every amino acid after deletion poin being incorrectlt (large affect)
Inversion mutation ONe codon is inverted in sequence. It results in a single amino acid change (minimal affect)
Basics of meitosis Cell duplicates chromosomes, chrom, line up in centre of cell, half the chromosones pulled to one side, the other the other side, cell splits in half in the middle. Each daughter cell is identcal
What are homologous chromosones Homologous chrom. are chromo,pairs of approx the same length, centromere position, and staining pattern, with genes for the same characteristics at corresponding loci.
Where are homolgous chromosones inherited from One homologous chromosome is inherited from the organism's mother; the other from the organism's fathe
WHen does chromosone crossing over happen homologous chromosomes pair up with each other and exchange different segments of their genetic material to form recombinant chromosomes. Crossing over is essential for the normal segregation of chromosomes during meiosis
Basics of meiosis Homologous pairs join up to form bivalents, crossing over can occur (recombination) as non-sister chromatids become entangled, two cell divisions to form 4 daughter cells that are haploid
diploid two copies of each chromosone (body cells)
haploid half he copies of each chromosone (gametes)
What are the different types of inheritence Dominant/recessive, Co-dominant, incomplete dominance, polygenics, multiple alleles
Dominant recesssive 2 pheontypes, all p traits (fly eyes, wrinkled coat) Aa
C0-dominant 3 phenotypes\.Roan cows - red and white at same time RW Both alles are dominant and contribute to phenotype
Incomplete dominance (blending/dilurtion) 3 phenotypes. e.g pink glowers RW
Polygenics Trait One trait but multiple gene loci. Usually dominant/recessive More than one gene determines phenotype and there is a dilution. e.g skin colour
Multiple alle.es more than 2 alles. E.g blood type there is A, B and O. One loci but multiple alles
Monohybrid crosses one gene - single gene inheritance
dihybrid crosses 2 genes
red hair and freckles close to each other on gene loci - so when swapping occurs both are expressed
Things close to each other on gene loci can be swapped in multiple crossing
AaBb heterozygous for both gene loci
wht would be the games of AaBb aB, bB, AB, ab.Aa or Bb can't go together due to meiosis (each allele for each gene loci)
what is autosomal not-sex linked
What is linkage genes thar located on the same chromosone. Linked genes tend to be inherited together (the extent of crossing over depends on how close together they are on the chromosone)
What is sex linkage Non-sexual traits coded by genes on X chromosone. y chromosone only dictates gener while x chromosone dictates gender and and other genes not related to sex
Why are males more prone to have sex linked diseases Males only need one mutation on allele to have the disorder (if dominant and recessive) while females need 2 therefore less incidents occur
What is linkage tendency of genes that are located close on a chrom. to be inherited together during meiosis. Genes whose loci are nearer to each other - less likely to be separated onto different chromatids during chromosomal crossover
when chromosones are doubled they form CHROMATID
Chromosones have sister chromatids which are joined at the centromere
Crossing over produces Variation - genetically different chromosones. Chromosones
What does natural selection depend on Variation in the gene pool
What creates variation Mutation, chromosonal crossing, sex, inheritance type
Selecting creates variation agent (helps organisms survive or doesn't). This results in directed change in gene pool. This requires generations (happens over extended period of time
What is speciation the formation of new and distinct species in the course of evolution. Caused by selecting pressures. Different species when they don't recognise each other
What does seperation do Different environments and selecting pressurese
What does isolation do new variants
what are the different types of isolation Geographical (continental drift, earthquakes - 2 different places at same time), temporal (same place but different times), reproductive (same place and time but don't recognise each other
What is stabilising selection Extreme variations are eliminated (so only middle of bell curve). And the middle phenotyes are retained in greater numbers. Acts to prevent divergence of form and function. E,g. birth weight
Directional Selection One extreme is eliminated and adaptie phenotype is shifted (one phenotype is favoured over the others). e.g. moth story
Disruptive selection Middle of bell curve is eliminated and two separate peaks form. Favours two extreme phenotypes at expense of intermediated forms.
In a karyotyoe how do you know if it'male or female The last homologous pair. If are equal sizes they are female. If one is shorter than the other it is shorter than it is male
How do they make karyotyoed White blood cells are frozen in the metaphase (lined up in the middle - the most dense and tangled) photo is taken and cut up so homologous pairs line up
What is endosymbiosis Symbiosis where one organism lives in another . Mitochondria and chloroplasts were once living bacteria until absorbed in eukaryotes
How are viruses are a mechanism of horizontal gene transfer Bacteriophages insert there DNA into bacteria . This viral DNA takes control of bacteria and bacteria produces thousands Iof the virus. The new viruses contain bacterial DNA . This is known as transduction
In RNA t is replaced with T is replaced with u
How can you tell the relatedness of an individual in gel electrophoresis Number of matching bands. Bottom to top. Cgta
How to read a codon table Left hand, up then right
Created by: Lui24
 

 



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