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Biology

Section 7 (Reproduction and Inheritance)

QuestionAnswer
What is a genome? The entire set of genetic material within an organism
What is a gene? A short section of DNA that codes for a specific protein
What is an allele? Different versions of the same gene
What does homozygous mean? When an organism has 2 of the same alleles
What does heterozygous mean? When an organism has 2 different alleles
What is a genotype? The two alleles present for a particular gene
What is a phenotype? Visible characteristics of an organism they get from the genotype
What is the structure of a DNA molecule? 2 strands of nucleotides making a double helix shape
What are the complementary base pairing rules in DNA? A-T and C-G
What is a mutation? A rare, random change to an organisms DNA
What might a mutation lead to? Could have effect of phenotype, altering characteristics slightly
How many chromosomes are there in each human cell? 46
How many chromosomes per cell do we get from each parent? 23
How many of each type of chromosome does a cell have? 2
Genes are the code for different sequences of ______________ amino acids
What is a disease called when it is caused by one of your genes? Inherited disease
The DNA in typical human cell is found in tight coils known as _________________ chromosomes
What are the sex chromosomes of women? XX
What are the sex chromosomes of men? XY
What are the 2 main differences between RNA and DNA? 1. RNA is single-stranded 2. RNA contains uracil instead of thymine
Where are chromosomes found in the cell? Nucleus
DNA is a ___________ , made up of many _____________ polymer, monomers
Each nucleotide has a ___________ on top, connected to a _______, with a ____________ on the side phosphate, sugar, base
In DNA, the structure formed by sugar and phosphates is called what? A sugar-phosphate backbone
What is it called when A-T and C-G bases pair up? Complimentary base pairing
What is a genetic code? A sequence of bases
Each set of three bases is called a _________, which code for an _____________ triplet, amino acid
What are the 3 main uses of proteins in the body? 1. Enzymes 2. Hormones 3. Structural proteins
What enzyme is involved in transcription? RNA Polymerase
What pairs with uracil on an mRNA strand? Adenine
What is a chain of amino acids called? A polypeptide
What are gametes? Sex cells
What does codominance mean? When both alleles in a genotype are expressed within the phenotype
What does it mean when a characteristic is polygenic? It is controlled by more than one gene
What is polygenic inheritance? When an organism inherits characteristics that are controlled by more than one gene
What is monohybrid inheritance? The inheritance of characteristics controlled by a single gene
Why are family pedigree diagrams useful? They can be used to trace inheritance patterns of a certain disease
How are each of these represented on a family pedigree diagram: 1. Affected male 2. Affected female 3. Unaffected male 4. Unaffected female 1. Red square 2. Red circle 3. Blue square 4. Blue circle
Who is responsible for determining the sex of a child? The father, as he is the only one with a Y chromosome
Sex is determined by a _____ of chromosomes pair (the 23rd pair)
The sperm that reaches the egg will either carry an _____ or a _____ chromosome, determining the gender of the child X, Y
Name 3 reasons why new cells are constantly required in an organism 1. Growth 2. Repair 3. Development (e.g. as new tissue develops)
What is the cell cycle? The series of steps that take place as a cell grows and then divides
What is a diploid cell? A cell with two copies of each chromosome
What do chromosomes do in a cell before division? Double
What does the term 'haploid' mean? A cell that only has half the normal amount of genetic material
Name 3 differences between mitosis and meiosis 1. 1 cell division / 2 cell divisions 2. 2 cells produced / 4 cells produced 3. Daughter cells are diploid / daughter cells are haploid
How is genetic variation between zygotes created? Through the different random fusions of gametes at fertilisation
Most mutations occur in _____________ DNA non-coding
What 2 factors can increase the risk of mutations? 1. Carcinogens (such as cigarettes) 2. Ionising radiation
Created by: JoeMather
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