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Biology revision Yr10
Biology revision Yr10

... father suffers from sickle cell anaemia – a recessive disease. Julie is normal but her family is known to suffer from this disease (let a = anaemia and A = normal). (i) Write down the genotypes of Jeff ____________ and Julie __________. (ii) Write down Jack’s genotype ___________. (iii) What gene di ...
Ch - TeacherWeb
Ch - TeacherWeb

... chromosomes found in the nucleus. 2. DNA located on the chromosomes is arranged in segments that control the protein production 3. genes: DNA segments that control protein production. 4. homologous chromosomes: chromosomes that make up a pair, one chromosome from each parent  humans = 46 chromosome ...
Biology 303 EXAM II 3/14/00 NAME
Biology 303 EXAM II 3/14/00 NAME

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... 4. Where are gametes located in the body? ______________________________________________________ 5. DNA in the ________________________ cells can be passed on to offspring. 6. What are homologous chromosomes? ______________________________________________________________________________________ 7. C ...
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... Law of Segregation. Non-homologous chromosomes account for Mendel's Law of Independent Assortment ...
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... – cross the organism with dominant character to an organism with homozygous recessive character – to test whether the organism with the dominant character is homozygous or heterozygous • Back cross – cross an organism with one of its parent ...
Chap 2. Biology of Propagation
Chap 2. Biology of Propagation

... • Autoploidy Multiplication of the complete set of genomes of a species • Alloploidy Polyploid containing genetically different sets of chromosomes derived from 2 or more species ...
B3 * student gap fill
B3 * student gap fill

... desired characteristics is removed and inserted into an ______ cell with its nucleus removed. The new egg cell is given an el_____ s_____ then divides to become an e_______ with the features of the organism the nucleus was taken from 2. Selective breeding is where organisms are breed to be less v_ ...
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Chapter 4 Genetics: The Science of Heredity C4S1 `Mendel`s Work

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IB Biology Topic 4: Genetics (15 hours)
IB Biology Topic 4: Genetics (15 hours)

... transcription and translation, using the example of sickle-cell anemia. GAG has mutated to _______________ Because of this mutation, glutamic acid is replaced by __________ How does this cause sickle cell anemia? ...
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BIO 220 Chapter 8 lecture outline Vocabulary Central dogma of

... Transduction Plasmids & transposons Objective questions 1. Be able to define all of the vocabulary used in lecture. 2. What is the central dogma of biology? Who proposed this theory? 3. What is the difference between the terms genotype and phenotype? Are bacteria typically diploid or haploid? What d ...
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4-3 Challenge Practice Questions

... • There are twice as many chromosomes in sex cells than in body cells. • False – There are half as many chromosomes in the sex cell as the body ...
GENERAL ZOOLOGY LECTURE EXAM 2
GENERAL ZOOLOGY LECTURE EXAM 2

... 12. If an organism's 2n number is 12, how many chromosomes will be present in each daughter cell at the end of meiosis II? a. 2 b. 6 c. 12 d. 24 e. 48 13. Can Mendel’s law of independent assortment be expected to hold true when the two sets of traits being examined are located on two different pairs ...
Biology 303 EXAM II 3/14/00 NAME
Biology 303 EXAM II 3/14/00 NAME

... 2. position effect. 3. nondisjunction. 4. genomic imprinting. ...
1. Describe the contributions that Thomas Hunt Morgan, Walter
1. Describe the contributions that Thomas Hunt Morgan, Walter

Cell Cycle
Cell Cycle

... G1 - cell grows and functions normally - high amount of protein synthesis occurs - more organelles are produced 2. S - DNA replication (doubles DNA) 3. G2 - cell growth continues ...
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Genetics

... individual and gives them a random shuffle. *This means an organism’s gametes are actually a new, totally unique combination of that individual’s own parents! ...
Faithful meiotic chromosome segregation in Caenorhabditis elegans
Faithful meiotic chromosome segregation in Caenorhabditis elegans

... Meiosis is the specialized cell division that is essential for the generation of haploid germ cells. It not only compensates for the doubling of chromosome number after fertilization but also generates genetic diversity by reciprocal exchange of paternal and maternal chromosome portions. Defects in ...
B2 Topic 1 The Components of Life
B2 Topic 1 The Components of Life

... What uses are there for genetic engineering? Bacteria Cell ...
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Meiosis

... • Two (diploid) parents give rise to offspring • Offspring differ genetically from their parents and their siblings • GAMETES are haploid reproductive cells that transmit genes across generations ...
Sex-linked traits
Sex-linked traits

... an inherited trait that has a gene on the x chromosome but no corresponding gene on the y chromosome (genes that only exist only on the sex chromosomes) ...
PPT
PPT

... • Two (diploid) parents give rise to offspring • Offspring differ genetically from their parents and their siblings • GAMETES are haploid reproductive cells that transmit genes across generations ...
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Chromosome



A chromosome (chromo- + -some) is a packaged and organized structure containing most of the DNA of a living organism. It is not usually found on its own, but rather is complexed with many structural proteins called histones as well as associated transcription (copying of genetic sequences) factors and several other macromolecules. Two ""sister"" chromatids (half a chromosome) join together at a protein junction called a centromere. Chromosomes are normally visible under a light microscope only when the cell is undergoing mitosis. Even then, the full chromosome containing both joined sister chromatids becomes visible only during a sequence of mitosis known as metaphase (when chromosomes align together, attached to the mitotic spindle and prepare to divide). This DNA and its associated proteins and macromolecules is collectively known as chromatin, which is further packaged along with its associated molecules into a discrete structure called a nucleosome. Chromatin is present in most cells, with a few exceptions - erythrocytes for example. Occurring only in the nucleus of eukaryotic cells, chromatin composes the vast majority of all DNA, except for a small amount inherited maternally which is found in mitochondria. In prokaryotic cells, chromatin occurs free-floating in cytoplasm, as these cells lack organelles and a defined nucleus. The main information-carrying macromolecule is a single piece of coiled double-stranded DNA, containing many genes, regulatory elements and other noncoding DNA. The DNA-bound macromolecules are proteins, which serve to package the DNA and control its functions. Chromosomes vary widely between different organisms. Some species such as certain bacteria also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm which contain cellular DNA and play a role in horizontal gene transfer.Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction plays a vital role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis leading to the progression of cancer.In prokaryotes (see nucleoids) and viruses, the DNA is often densely packed and organized. In the case of archaea by homologs to eukaryotic histones, in the case of bacteria by histone-like proteins. Small circular genomes called plasmids are often found in bacteria and also in mitochondria and chloroplasts, reflecting their bacterial origins.
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