* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Chapter 10 Study Guide Know the definitions for: Cross
Non-coding RNA wikipedia , lookup
DNA sequencing wikipedia , lookup
Human genome wikipedia , lookup
Nucleic acid tertiary structure wikipedia , lookup
History of RNA biology wikipedia , lookup
Zinc finger nuclease wikipedia , lookup
Mitochondrial DNA wikipedia , lookup
Comparative genomic hybridization wikipedia , lookup
DNA profiling wikipedia , lookup
Genomic library wikipedia , lookup
Expanded genetic code wikipedia , lookup
Messenger RNA wikipedia , lookup
Cancer epigenetics wikipedia , lookup
DNA polymerase wikipedia , lookup
No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing wikipedia , lookup
Genetic code wikipedia , lookup
SNP genotyping wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Genealogical DNA test wikipedia , lookup
Gel electrophoresis of nucleic acids wikipedia , lookup
Bisulfite sequencing wikipedia , lookup
DNA vaccination wikipedia , lookup
United Kingdom National DNA Database wikipedia , lookup
Epitranscriptome wikipedia , lookup
Molecular cloning wikipedia , lookup
DNA damage theory of aging wikipedia , lookup
History of genetic engineering wikipedia , lookup
Epigenomics wikipedia , lookup
Microevolution wikipedia , lookup
Non-coding DNA wikipedia , lookup
Microsatellite wikipedia , lookup
Cre-Lox recombination wikipedia , lookup
Extrachromosomal DNA wikipedia , lookup
Frameshift mutation wikipedia , lookup
Therapeutic gene modulation wikipedia , lookup
Cell-free fetal DNA wikipedia , lookup
DNA supercoil wikipedia , lookup
Primary transcript wikipedia , lookup
Nucleic acid double helix wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Helitron (biology) wikipedia , lookup
Deoxyribozyme wikipedia , lookup
Chapter 10 Study Guide Know the definitions for: Cross-over Genotype Phenotype Homozygous Heterozygous Genetics Independent assortment Haploid Diploid Triploid Tetraploid Sperm Egg Gamete Pollination Fertilization Meiosis Alleles Dominant Recessive Dihybrid Heredity Zygote How do you set up a Punnett square for a monohybrid or dihybrid cross given the parents genotypes? (What are the potential genotypes of the gametes?) Be able to utilize a Punnett square for a monohybrid and dihybrid crosses and give the genotypes and phenotypes of potential offspring (plus the ratios). Chapter 11 Study Guide Know the definition / application of the following terms: chromosomal mutation frameshift mutation replication codon mRNA translation cytosine nitrogen bases translocation double helix point mutation tRNA _?_ & _?_ were the first to suggest that DNA is the shape of a double helix. Be able to draw and label the structure of a nucleotide and DNA ladder: Backbone or sides of the DNA ladder composed of _?_ & _?_ Rungs of DNA ladder composed of _?_ _?_ Nitrogen bases of DNAPurines (double-ring structure) consist of _?_ (G) & _?_ (A) Pyrimidines (single-ring structure) consist of _?_ (T) & _?_ (C) Within the DNA ladder; Adenine always pairs with _?_ , and Cytosine always pairs with _?_ Be able to describe the process of DNA replication (DNA making exact copy of itself). Be able to put the following in order of size (DNA, cell, nucleotide, nucleus, chromosome). RNA (like DNA) is also composed of nucleotides, but the RNA strand differs from DNA: Single-strand (not double-stranded) Ribose sugar (not deoxyribose sugar) Uracil nitrogen base (in place of thymine) Exist in three forms: mRNA – transcription of DNA sequence that can move from the nucleus to cytoplasm to site of ribosomes. tRNA – translation of mRNA sequence carried from the nucleus by carrying appropriate amino acids to construct polypeptide sequence (protein). rRNA – ribosomes are composed of rRNA and protein that provides site for translation of DNA code to construct protein sequence. Study diagram on page 294 to better understand translation. Mutagens are X rays, ultraviolet light, and radioactive substances that can change the chemical nature of DNA. Frameshift mutation occurs when a nucleotide is added or removed from a DNA molecule and mRNA is created, the codons after the mutation will not be read correctly resulting is different amino acids coded for.(i.e. = -AATTACGGCATA- is changed to – ATTACGGCATA-) Point mutation occurs when a single nitrogen base is changed (i.e. = -ATCGGA- is changed to –ACCGGA-) that result in a difference in amino acid coded for and perhaps the structure and function of final protein. Translocation is a chromosomal abnormality that occurs when part of one chromosome breaks off and is added to a different chromosome.