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Cellular Basis of Life The Cell Cycle Growth, Repair, & Reproduce

  1. All cells come from other cells 2. The division of cells allows living things to: Repair damage Grow Reproduce offspring Asexual Sexual Chromosomes

  2. DNA usually exists in the nucleus as chromatin “string” Before cells divide, DNA duplicates & and condenses Chromosomes are DNA wound around proteins (histones) Sister chromatids joined at the centromere The Cell Cycle

  3. Interphase (90%): cell does normal cell activities and: G1- increases proteins, organelles, and size S- duplicates DNA G2- increases supplies for cell division 2. Mitotic phase- division of cell * Mitosis (M)- nucleus divides (PMAT) Cytokinesis- cytoplasm divides The Mitotic Phase The Stages of Mitosis

  4. Prophase- DNA condenses Nucleus disappears Spindle fibers appear and attach to kinetochores 2. Metaphase- DNA lines up in the middle 3. Anaphase- DNA separates

  5. Telophase- Opposite of Prophase Cytokinesis

  6. Animal cells pinch in the middle (cleavage furrow)

  7. Plant cells form a cell plate in the middle

New cells are called daughter cells. Reproduction in Prokaryotes

  1. Binary fission- 1 cell divides into 2 daughter cells Asexual reproduction Divide every 20 minutes Sexual Reproduction Homologous Chromosomes

  2. Chromosomes can be examined by amniocentesis The display of the chromosomes is called karyotype 2. Each chromosome has a twin referred to as a homologous chromosome homologous pairs contain the same type of information The genes may have different versions of the same trait Ex: (eyes: blues/brown) Diploid and Haloid Cells

    1. Diploid cells (2n) have two sets of homologous chromosomes Human’s body cell (46) 23 homologous pairs (numbered 1-23) One set from each parent Pair #23 are the sex chromosomes Female- XX Male- XY All the other pairs called autosomes

  3. Haploid cells (n) have one set of chromosomes Human sex cells (23) 3. When two sex cells (gametes) are joined (fertilization) a zygote is formed Cancer

  4. Benign tumor is a mass of normal cells

  5. Malignant tumor is a mass of cancer cells Cancer is a disease caused when cells divide and grow out of control When cancer spreads, it is called metastasis Cancer is treated by: Radiation Chemotherapy Meiosis & Variations The Stages of Meiosis

  6. Meiosis I: separation of homologous pairs Prophase I: Crossing over b/w homologous pairs Metaphase I: homologous pairs line up Anaphase I: homologous pairs separate Telophase I: homologous pairs sometimes relax (interkinesis)

  7. Meiosis II (same as mitosis): separation of sister chromatids Causes of Genetic Variations

    1. Crossing over Synapsis occurs by forming tetrads Exchange of DNA between homologous pairs Different chromosomes are produced through genetic recombination

    2. Independent assortment Homologous pairs of chromosomes are separated randomly 2n possible combinations of 223 = 8 million Mitosis vs. Meiosis

    3. Mitosis produces: 2 cells Diploid (2n) genetically identical

    4. Meiosis produces: 4 cells Haploid genetically different

Patterns of Inheritance The Language of Genetics History

  1. The blending hypothesis of the 1800s was discarded

  2. Gregor Mendel, the “father of genetics” believed that distinct factors (genes) were responsible for inheritance Conducted breeding experiments on pea plants 3. Genetics- the study of how traits are passed from parent to offspring The Rules of Chance

    1. Gene- a portion of the chromosome that controls a trait (flower color)

    2. Allele- Either one of the alternate versions of a gene (P or p) Genotype- genetic composition (PP or Pp or pp) Phenotype- physical appearance (purple or white)

    3. True-breed- an organism that always passes on it characteristics Homozygous- two of the same alleles for the same trait

  3. Hybrid- an organism that has two different alleles for the same trait Heterozygous- two different alleles for the same trait 5. Dominant- in a hybrid, the allele that is expressed (P-purple) 6. Recessive- in hybrid, the allele that is not expressed (p- white) 7. P Generation- parents (PP x pp) 8. F1 Generation- Children (4/4 Pp) 9. F2 Generation- grandchildren (¼ PP, ½ Pp, ¼ pp) Punnet Squares Mendel’s Laws

    1. Individual units, called genes, determine biological characteristics

    2. For each gene, an organism receives one allele from each parent Alleles separate from each other (segregation) Forming sex cells

  4. If an organism inherits different alleles for the same trait, one allele is dominant over the other. 4. Some genes separate, or segregate independently Monohybrid Cross

    1. A monohybrid cross results from crossing two organisms that differ in one characteristic Identify the dominant and recessive alleles Determine the genotype of each parent and possible gametes Set up a Punnet square and cross List the genotypes and phenotypes of the offspring in each box Determine the solution to the problem Dihybrid Cross

  5. A dihybrid cross results from crossing organisms that differ in two characteristicsSeed color and shape Seed color and shape A cross between two hybrids results in a 9:3:3:1 ratio

Inheritance Patterns Incomplete Dominance 1. Incomplete dominance is when neither gene is totally dominant 2. Produces an intermediate phenotype Multiple Alleles 1. There are 4 blood types, A, B, AB, and O Type A Type AA Type Ao Type B Type BB Type Bo Type AB Type O 2. The gene for o is recessive to A and B 3. A and B are codominant 4. Mixing blood types can result in blood clotting Polygenic Inheritance 1. Polygenic inheritance is when more than one gene affects a single trait. Height and skin color 2. Produces a broad range of phenotypes

Environmental Influences 1. The environment can affect an individual's phenotype Height and weight, coloring, blood count

DNA: The Language of Life (Chapter 11 Lesson) The Structure of DNA History

  1. DNA- Deoxyribonucleic Acid Hereditary material of the cell Makes up genes Determines the traits of all living things Located in the nucleus Nucleotides

    1. DNA (polymer) is composed of long chains of four different nucleotides (monomers)

    2. Each nucleotide has: phosphate group sugar (deoxyribose) nitrogenous base adenine A thymine T guanine G cytosine C

  2. Adenine and Guanine are Purines (2 rings)

  3. Thymine and Cytosine are Pyrimidines (1 ring)

  4. DNA strands form when nucleotides join together Repeating sugar-phosphate “Backbone” nitrogenous bases are lined up 6. Two strands join together by hydrogen bonds The Double Helix

    1. Franklin & Wilkins and Watson & Crick determine the structure

    2. DNA resembles a twisted ladder Sugar-phosphate on the outside Complementary nitrogenous bases pair on the inside A - T C - G DNA Replication & Mutations DNA Replication

    3. Replication is the process used to make a copy of DNA

    4. During DNA replication: The two complementary strands separate to form templates Free nucleotides line up with complementary bases New strands are covalently bonded Enzymes control the process Replication is semi-conservative Protein Production From Gene to Protein

  5. For every gene (recipe) there is a protein

  6. Proteins determine the appearance and function of the cell/ organism

  7. DNA → RNA → protein Transcription Translation 4. The genetic code consists of 3 letter codes (codon) Each condon stands for a particular amino acid “All” organisms share this code RNA

  8. RNA (Ribonucleic Acid) differs from DNA: Sugar (ribose) Single Strand 2. Types of RNA mRNA (message) copy of the recipe rRNA (ribosome) stove tRNA (transfer) utensils Transcription

  9. Transcription is the process of converting the information of DNA onto mRNA Similar to DNA replication except: Uses RNA nucleotides (U pairs with A) Only 1 gene is copied mRNA leaves the nucleus Translation

  10. Translation is the process of converting information of mRNA into a protein tRNA acts as the translator b/w nucleic acids and proteins The ribosome is the meeting place for mRNA and tRNA

  11. Steps in reading mRNA: AUG is the code for start As each code word is read, amino acids are added UAA, UAG, or UGA are the codes for stop 3. Protein is completed and released Sex-linked Traits

    1. Sex chromosomes carry genes for traits Some genes are located on the X chromosomes (females have 2 genes) Males have only 1 gene for each of these traits

    2. Thomas Hunt Morgan discovered sex-linked traits (eye color) in fruit flies

Cellular Basis of Life The Cell Cycle Growth, Repair, & Reproduce

  1. All cells come from other cells 2. The division of cells allows living things to: Repair damage Grow Reproduce offspring Asexual Sexual Chromosomes

  2. DNA usually exists in the nucleus as chromatin “string” Before cells divide, DNA duplicates & and condenses Chromosomes are DNA wound around proteins (histones) Sister chromatids joined at the centromere The Cell Cycle

  3. Interphase (90%): cell does normal cell activities and: G1- increases proteins, organelles, and size S- duplicates DNA G2- increases supplies for cell division 2. Mitotic phase- division of cell * Mitosis (M)- nucleus divides (PMAT) Cytokinesis- cytoplasm divides The Mitotic Phase The Stages of Mitosis

  4. Prophase- DNA condenses Nucleus disappears Spindle fibers appear and attach to kinetochores 2. Metaphase- DNA lines up in the middle 3. Anaphase- DNA separates

  5. Telophase- Opposite of Prophase Cytokinesis

  6. Animal cells pinch in the middle (cleavage furrow)

  7. Plant cells form a cell plate in the middle

New cells are called daughter cells. Reproduction in Prokaryotes

  1. Binary fission- 1 cell divides into 2 daughter cells Asexual reproduction Divide every 20 minutes Sexual Reproduction Homologous Chromosomes

  2. Chromosomes can be examined by amniocentesis The display of the chromosomes is called karyotype 2. Each chromosome has a twin referred to as a homologous chromosome homologous pairs contain the same type of information The genes may have different versions of the same trait Ex: (eyes: blues/brown) Diploid and Haloid Cells

    1. Diploid cells (2n) have two sets of homologous chromosomes Human’s body cell (46) 23 homologous pairs (numbered 1-23) One set from each parent Pair #23 are the sex chromosomes Female- XX Male- XY All the other pairs called autosomes

  3. Haploid cells (n) have one set of chromosomes Human sex cells (23) 3. When two sex cells (gametes) are joined (fertilization) a zygote is formed Cancer

  4. Benign tumor is a mass of normal cells

  5. Malignant tumor is a mass of cancer cells Cancer is a disease caused when cells divide and grow out of control When cancer spreads, it is called metastasis Cancer is treated by: Radiation Chemotherapy Meiosis & Variations The Stages of Meiosis

  6. Meiosis I: separation of homologous pairs Prophase I: Crossing over b/w homologous pairs Metaphase I: homologous pairs line up Anaphase I: homologous pairs separate Telophase I: homologous pairs sometimes relax (interkinesis)

  7. Meiosis II (same as mitosis): separation of sister chromatids Causes of Genetic Variations

    1. Crossing over Synapsis occurs by forming tetrads Exchange of DNA between homologous pairs Different chromosomes are produced through genetic recombination

    2. Independent assortment Homologous pairs of chromosomes are separated randomly 2n possible combinations of 223 = 8 million Mitosis vs. Meiosis

    3. Mitosis produces: 2 cells Diploid (2n) genetically identical

    4. Meiosis produces: 4 cells Haploid genetically different

Patterns of Inheritance The Language of Genetics History

  1. The blending hypothesis of the 1800s was discarded

  2. Gregor Mendel, the “father of genetics” believed that distinct factors (genes) were responsible for inheritance Conducted breeding experiments on pea plants 3. Genetics- the study of how traits are passed from parent to offspring The Rules of Chance

    1. Gene- a portion of the chromosome that controls a trait (flower color)

    2. Allele- Either one of the alternate versions of a gene (P or p) Genotype- genetic composition (PP or Pp or pp) Phenotype- physical appearance (purple or white)

    3. True-breed- an organism that always passes on it characteristics Homozygous- two of the same alleles for the same trait

  3. Hybrid- an organism that has two different alleles for the same trait Heterozygous- two different alleles for the same trait 5. Dominant- in a hybrid, the allele that is expressed (P-purple) 6. Recessive- in hybrid, the allele that is not expressed (p- white) 7. P Generation- parents (PP x pp) 8. F1 Generation- Children (4/4 Pp) 9. F2 Generation- grandchildren (¼ PP, ½ Pp, ¼ pp) Punnet Squares Mendel’s Laws

    1. Individual units, called genes, determine biological characteristics

    2. For each gene, an organism receives one allele from each parent Alleles separate from each other (segregation) Forming sex cells

  4. If an organism inherits different alleles for the same trait, one allele is dominant over the other. 4. Some genes separate, or segregate independently Monohybrid Cross

    1. A monohybrid cross results from crossing two organisms that differ in one characteristic Identify the dominant and recessive alleles Determine the genotype of each parent and possible gametes Set up a Punnet square and cross List the genotypes and phenotypes of the offspring in each box Determine the solution to the problem Dihybrid Cross

  5. A dihybrid cross results from crossing organisms that differ in two characteristicsSeed color and shape Seed color and shape A cross between two hybrids results in a 9:3:3:1 ratio

Inheritance Patterns Incomplete Dominance 1. Incomplete dominance is when neither gene is totally dominant 2. Produces an intermediate phenotype Multiple Alleles 1. There are 4 blood types, A, B, AB, and O Type A Type AA Type Ao Type B Type BB Type Bo Type AB Type O 2. The gene for o is recessive to A and B 3. A and B are codominant 4. Mixing blood types can result in blood clotting Polygenic Inheritance 1. Polygenic inheritance is when more than one gene affects a single trait. Height and skin color 2. Produces a broad range of phenotypes

Environmental Influences 1. The environment can affect an individual's phenotype Height and weight, coloring, blood count

DNA: The Language of Life (Chapter 11 Lesson) The Structure of DNA History

  1. DNA- Deoxyribonucleic Acid Hereditary material of the cell Makes up genes Determines the traits of all living things Located in the nucleus Nucleotides

    1. DNA (polymer) is composed of long chains of four different nucleotides (monomers)

    2. Each nucleotide has: phosphate group sugar (deoxyribose) nitrogenous base adenine A thymine T guanine G cytosine C

  2. Adenine and Guanine are Purines (2 rings)

  3. Thymine and Cytosine are Pyrimidines (1 ring)

  4. DNA strands form when nucleotides join together Repeating sugar-phosphate “Backbone” nitrogenous bases are lined up 6. Two strands join together by hydrogen bonds The Double Helix

    1. Franklin & Wilkins and Watson & Crick determine the structure

    2. DNA resembles a twisted ladder Sugar-phosphate on the outside Complementary nitrogenous bases pair on the inside A - T C - G DNA Replication & Mutations DNA Replication

    3. Replication is the process used to make a copy of DNA

    4. During DNA replication: The two complementary strands separate to form templates Free nucleotides line up with complementary bases New strands are covalently bonded Enzymes control the process Replication is semi-conservative Protein Production From Gene to Protein

  5. For every gene (recipe) there is a protein

  6. Proteins determine the appearance and function of the cell/ organism

  7. DNA → RNA → protein Transcription Translation 4. The genetic code consists of 3 letter codes (codon) Each condon stands for a particular amino acid “All” organisms share this code RNA

  8. RNA (Ribonucleic Acid) differs from DNA: Sugar (ribose) Single Strand 2. Types of RNA mRNA (message) copy of the recipe rRNA (ribosome) stove tRNA (transfer) utensils Transcription

  9. Transcription is the process of converting the information of DNA onto mRNA Similar to DNA replication except: Uses RNA nucleotides (U pairs with A) Only 1 gene is copied mRNA leaves the nucleus Translation

  10. Translation is the process of converting information of mRNA into a protein tRNA acts as the translator b/w nucleic acids and proteins The ribosome is the meeting place for mRNA and tRNA

  11. Steps in reading mRNA: AUG is the code for start As each code word is read, amino acids are added UAA, UAG, or UGA are the codes for stop 3. Protein is completed and released Sex-linked Traits

    1. Sex chromosomes carry genes for traits Some genes are located on the X chromosomes (females have 2 genes) Males have only 1 gene for each of these traits

    2. Thomas Hunt Morgan discovered sex-linked traits (eye color) in fruit flies