genetics and genomics

    Cards (74)

    • What is the focus of genomics?
      Genomics is the study of all the genes in our DNA.
    • How does genomics differ from genetics?
      Genetics studies single genes, while genomics studies all genes in the genome.
    • When did the scientific history of genetics begin?
      In the 1860s.
    • When was the human genome sequenced?
      In 2003.
    • What does epigenetics explain?
      It explains how different types of cells are formed from the same genome.
    • How does epigenetics influence gene expression?
      It regulates which genes are expressed without changing the DNA itself.
    • How can the epigenome of a developing baby be influenced?
      By the expectant parent's lifestyle while still in the womb.
    • What is the genome found in?
      Deoxyribonucleic acid (DNA).
    • How many chromosomes do humans have?
      46 chromosomes.
    • What are genes?
      Specific sequences of DNA.
    • What do coding genes do?
      They code for proteins required by the body to function and reproduce.
    • What do non-coding genes do?
      They act as regulators for protein synthesis.
    • What is DNA synthesized from?
      Nucleotides.
    • What structure does DNA form?
      A double helix.
    • How do DNA bases pair?
      Adenine (A) pairs with thymine (T) and guanine (G) pairs with cytosine (C).
    • What are the main steps of protein synthesis?
      1. Gene expression: using the genetic code to synthesize proteins.
      2. Transcription: transfer of genetic information from DNA to messenger RNA (mRNA).
      3. Translation: reading mRNA to synthesize the corresponding protein.
    • What are chromosomes made of?
      DNA and proteins.
    • When can chromosomes be observed?
      During the metaphase of cell division.
    • What type of cells are diploid?
      Cells that contain 2 copies of each chromosome.
    • What are gametes?
      Haploid cells that contain 1 copy of each chromosome.
    • What is created when an ovum is fertilized by a sperm?
      A zygote.
    • What are the phases of mitosis?
      1. Prophase: Chromatin organizes into chromosomes.
      2. Metaphase: Chromosomes align at the cell center.
      3. Anaphase: Sister chromatids separate to opposite ends.
      4. Telophase: Nuclear membranes form around each set of chromosomes.
      5. Cytokinesis: Plasma membrane forms between the two new nuclei.
    • What are the stages of meiosis?
      1. Meiosis 1:
      • Prophase 1: Chromosomes align and recombination occurs.
      • Metaphase 1: Chromosome pairs align at the cell center.
      • Anaphase 1: Chromosome pairs separate.
      1. Meiosis 2: Similar to mitosis, resulting in 4 unique daughter cells.
    • What is the purpose of meiosis?
      To produce gametes containing one chromosome from each of the 23 pairs.
    • What is recombination in meiosis?
      Exchanging segments of DNA between homologous chromatids.
    • What is independent assortment in meiosis?
      Random distribution of homologous pairs to create genetic variation.
    • What is a mutation?
      A mistake during DNA copying that changes the base sequence.
    • Where do most mutations occur?
      In the non-coding area of DNA.
    • What can mutations cause?
      They can cause cancer or cell death.
    • How can mutations be inherited?
      They can occur during a person's life or be inherited from parents.
    • What factors can increase the frequency of mutations?
      Radiation, ultraviolet light, alcohol, and tobacco.
    • From whom are new gene mutations predominantly inherited?
      From the father.
    • What is the spontaneous mutation rate in sperm compared to ovum?
      It is higher in sperm than in ovum.
    • What is associated with increasing paternal age regarding mutations?
      New paternal gene mutations.
    • What are alleles?
      Different types of each gene.
    • What does heterozygous mean?
      Having 2 different alleles inherited.
    • What does homozygous mean?
      Having 2 identical alleles inherited.
    • What is a genotype?
      All the genes present in an individual's cells.
    • What is a phenotype?
      Observable characteristics determined by an individual's genotype.
    • What causes single gene disorders?
      A mutation of a single gene.