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Chapters 10 - 13
These flashcards are from my 9th grade Biology class on Heredity
Question | Answer |
---|---|
Define heredity | When parents pass characteristics on to their offspring. |
Define traits | Inherited characteristics. |
Define genetics | The study of heredity. |
Define gametes | Male and female sex cells. |
Define zygote | A fertilized cell. |
Define pollination | When a male reproductive organ passes on to a female reproductive organ (occurs in plants.) |
Define hybrid | When an offspring has different forms of a trait. |
Define alleles | Alternate gene forms. |
Define dominant | The observed trait. |
Define recessive | The "disappearing" trait. |
What is the law of segregation? | That every individual has 2 alleles of each gene and when gametes are produced, each gamete receives one of these alleles. |
Define phenotype | How an organism looks and behaves (the prominent characteristics.) |
Define genotype | The allele combination of an organism. |
Define homozygous | 2 alleles are the same. |
Define heterozygous | When the 2 alleles are different (one dominant and 1 recessive in most cases.) |
What is the law of independent assortment? | When genes for 2 different traits are inherited independently of each other. |
How did Gregor Mendel discover the roles of genetics? | By crossing pea plants. |
How did Gregor Mendel perform his experiment? | He made a cross by removing the male parts of a flower, and transferring the male pollen grains of another flower and placing them on the female flower with the removed male parts. |
Define diploid | A cell with 2 kinds of each chromosome. |
Define haploid | A cell with 1 of each chromosome. |
What is a homologous chromosome? | 2 chromosomes of each pair in a diploid cell. |
Define meiosis | The part of cell division that produces gametes with 1/2 of the same number of chromosomes in the parents. |
Define sperm | Male gametes. |
Define eggs | Female gametes. |
Define sexual reproduction | When haploid sex cells come together. |
Define crossing over | When non - sister chromatids from homologous chromosomes break and exchange genetic material. |
Define genetic recombination | Chromosomes are re-assorted and their genetic information... |
Define nondisjunction | When homologous chromosomes don't separate properly during meiosis I. |
Name the stages of meiosis I and II. | Interphase-Prophase I-Metaphase I-Anaphase I-Telophase I-Prophase II-Metaphase II-Anaphase II-Telophase II |
Define nucleotide | Subunit of a nucleic acid formed form a simple sugar, a phosphate group, and a nitogenous base. |
Define nitrogenous base | A carbon ring structure that contains 1+ nitrogen atoms. |
Define double helix | 2 strands twisted together (DNA's shape). |
Define DNA replication | When DNA in the chromosomes is copied. |
What does DNA stand for? | Deoxyrobonucleic acid. |
What is DNA composed of? | A simple sugar, a phosphate group and a nitrogenous base. |
What do nucleotides bond to? | They bond to deoxyribose sugars. |
Define polymer | A large molecule formed from smaller subunits that are bonded together. |
What does messenger RNA do? | It brings instructions from DNA in the nucleus to the cytoplam. |
What does ribosomal RNA do? | It binds to the mRNA and uses instructions to assemble the amino acids correctly. |
What does transfer RNA do? | It delivers amino acids to the ribosome so that they can be made into proteins. |
Define transcription | When enzymes (in the nucleus) make a RNA copy of a strand of DNA. |
Define translation | When the nitrogenous base sequence in mRNA convert into an amino acid sequence (the amino acids in protein.) |
Define cancer | Diseases caused by changes in genes (control the cell cycle.) |
Define mutation | Any change in a DNA sequence. |
Define point mutation | A change in 1 base pair of DNA. |
Define frameshift mutation | Shifts all of the codon readings by one base. |
Define chromosomal mutations | They are more common in pants than animals - they create structure changes in the chromosomes. |
Define mutagen | Any factor that changes DNA. |
Why to mutagens in the eggs and sperms affect the offspring? | Because it is given new characteristics. |
Define trait | Any type of inherited characteristic. |
Define pedigree | A graphic representation of genetic inheritance. |
Define carrier | A heterozygous individual. |
Define fetus | A still developing baby. |
Can genetic disorders be inherited as dominant alleles? | Yes. |
Define incomplete dominance | When the allele for a specific trait is not completely dominant over the other allele. |
Define codominant alleles | When the phenotypes of 2 homozygous traits become heterozygous. |
Define multiple alleles | Traits that are controlled by more that 2 alleles. |
Define sex chromosomes | X & Y male=XY female=XX |
Define autosomes | 22 pairs of homologous chromosomes |
Define sex - linked traits | Traits controlled by genes in sex chromosomes. |
Define polygenic inheritance | The pattern of a trait controlled by 2+ genes. |
What are some traits affected by? | Internal and external conditions. |
Define karyotype | A chart of chromosome pairs - they are used to identify unusual chromosome numbers in cells. |
Define sickle - cell anemia | The red blood cells are misshapen because of the narrow capillaries. They slow blood flow, block small vessels, and result in tissue damage and pain. |
Define hemophilia | An X linked disorder, and it causes problems with blood clotting (slows down how fast your cut will heal.) |
Define test crosses | The cross of an individual and unknown genotype with a known genotype. |
Define genetic engineering | Faster and more reliable methos to increase the frequency of specific alleles. |
Define recombinant DNA | Connecting, or recombining fragments of DNA from various sources. |
Define transgenic organisms | They contain forgein DNA. |
Define plasmid | A small ring of DNA found in a bacterial cell. |
Define clone | Genetic identical copies. |
Define human genome | 35,000 - 40,000 genes on the 46 human chromosomes. |
Define linkage map | A genetic map that shows the relative locations of genes on a chromosome. |
Define gene therapy | The insertion of normal genes into human cells to correct genetic disorders. |