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65 Cards in this Set

  • Front
  • Back
Eukaryote
- cells contain their genetic material inside a nucleus
- includes large, complex organisms
- nucleus separates transcription and translation
- undergoes mitosis and meiosis
Nucleotide
- basic chemical unit in nucleic acids
- four nucleotides make up DNA
- if nucleotide sequence altered, protein may be altered
- purines = adenine and guanine
- pyrimidines = cytosine and thymine
Base Pairs
- pair of nucleotides form by complementary base pairing of a purine and pyrimidine
- A --> T
- G --> C
- surfaces are chemically distinct, allowing other specific molecules to bind to them
Chargaff's Rule
- A = T and G = C
- Total # of Purines = Total # of Pyrimidines
Double Helix
- stores an organism's genetic information
- right-handed
- antiparallel
- minor and major grooves
- sugar-phosphate "backbones" held together by hydrogen bonding
- complimentary base pairing
- 5' end = free, phosphate
- 3' end = free, hydroxyl
Genome
- the full DNA sequence of an organism
- divided into pieces called chromosomes
- haploid set of chromosomes in a gamete
- remains constant, but gene expression varies in space and time
Eukaryotic Genome
- larger --> more protein-coding genes
- contain numerous repetitive DNA sequences that do not code for polypeptides
Chromosomes
- the DNA molecule that contains most or all of the genetic information of a cell or virus
- chromosome number and structure can change without having a major effect on genome size or content
- has an ori, centromere region, and telomeric sequence to maintain chromosome integrity
Barr body
- one of X chromosomes in each cell of female is transcriptionally inactivated in early embryonic development
- reason why transcription is nearly same in both males and females
Sister Chromatids
- each of a pair of newly replicated chromatid
- after replication --> held together by cohesin
- by metaphase --> cohesin removed, except for at centromere
- by anaphase --> the enzyme separase hydrolyzes the remaining cohesin and chromosome separate
Haploid
- having a chromosome complement consisting of just one copy of each chromosome
- two haploid gametes fuse to form a zygote in fertilization
Diploid
- having a chromosome complement consisting of two copies of each chromosome
- zygotes are diploid --> may divide either by meiosis or mitosis --> new mature organism develops that is capable of sexual reproduction
Aneuploidy
- a condition in which one or more chromosomes or pieces of chromosomes are either lacking or present in excess
- trisomic of chromosome 21 = Down syndrome
Polyploidy
- the possession of more than two entire sets of chromosomes
- may be produced by artificial breeding or by natural accidents
- desirable trait in plants because leads to more robust plants
Duplication
- a mutation in which a segment of a chromosome is duplicated, often by the attachment of a segment lost from its homolog
- would arise if homologous chromosomes broke at different positions and reconnected to the wrong partners
Deletion
- result form the removal of part of the genetic material
- consequences can be severe unless they affect noncoding DNA or unnecessary genes
Inversion
- a segment of DNA may be removed and reinserted into the same location in chromosome, but "flipped" end over so that it runs in the opposite direction
- can result from breaking and rejoining of chromosomes
Reciprocal Translocation
- interchange of chromosome segments between two non-homologous chromosomes
Gene
- a unit of genetic function which carries the information for a single polypeptide or RNA
One-gene, One-enzyme Relationship
- genes act through the production of enzymes, with each gene responsible for producing a single enzyme that in turn effects a single step in a metabolic pathway
One-gene, One-polypeptide Relationship
- the function of a gene is to inform the production of a single, specific polypeptide
Transcription
- the information in a DNA sequence is copied into a complementary RNA sequence
Translation
- the process by which a sequence of nucleotide triplets in a mRNA gives rise to a specific sequence of amino acids during protein synthesis
Amino Acid
- an organic compound containing both NH2 and COOH groups
- proteins are polymers of amino acids
Adapter Molecule
- contains an anticodon complementary to the codon in mRNA
- binds a specific amino acid and recognizes a specific sequence of nucleotides
Protein
- long-chain polymer of amino acids with twenty different common side chains
Ribosome
- a small particle in the cell that is the site of protein synthesis
Polypeptide
- a large molecule made up of many amino acids joined by peptide linkages
- large polypeptides are called proteins
Messenger RNA (mRNA)
- carries a copy of a gene sequence in DNA to the site of protein synthesis at the ribosome
- must be translated in the correct reading frame
Ribosomal RNA (rRNA)
- catalyzes peptide bond formation and provides structural framework for the ribosome
Transfer (tRNA)
- carries amino acids to the ribosome for assembly into polypeptides
- charged tRNA will deliver appropriate amino acid to join the elongating polypeptide product of translation
- must read mRNA codons correctly
- must deliver the amino acids that correspond to each mRNA codon
microRNA
- a small, noncoding RNA molecule that binds to mRNA to inhibit its translation
- important regulators of gene expression
RNA Polymerase II
- enzyme in eukaryotic cells that catalyzes the transcription of DNA to synthesis precursors of mRNA, most snRNA, and microRNA
Transcription Factors
- binds to specific DNA sequences, thereby controlling the movement of genetic information from DNA to mRNA
- allows RNA Polymerase II to perform transcription
TATA Box
- a promoter DNA sequence crucial in forming the transcription intiation complex
Exon
- portion of DNA molecule that codes for part of a polypeptide
- expressed regions
- interspersed with the coding sequences
Intron
- portion of a coding region in gene that is transcribed into pre-mRNA but is spliced out prior to translation
- intervening regions
- interrupt, but do not scramble DNA sequence
Splicing
- transcripts of introns are excised through the action of snRNPs
- last stage of RNA processing in eukaryotes
- increases protein diversity
Spliceosome
- result of binding of snRNPs to consensus sequences bordering the introns on the pre-mRNA
- series of proteins binding
Start Codon
- the mRNA triplet (AUG) that acts as a signal for the beginning of translation at the ribosome
- contains three consecutive nucleotides
- determines reading frame
Initiator tRNA
- initiates protein synthesis by binding to the amino acid methionine and delivering it to the small ribosomal unit
- employed in initiation step of protein synthesis
- attaches to ribosome's P site
Stop Codon
- any of the three mRNA codons that signal the end of protein translation at the ribosome
- UAG, UGA, UAA
Epigenetics
- the scientific study of changes in the expression of a gene or set of genes that occur without change in the DNA sequence
- changes are reversible, but sometimes stable and hereditary
- includes DNA methylation and chromosomal protein alterations
Histones
- DNA is wrapped around it to produce chromatin
- forms core of nucleosome
- the structural unit of a eukaryotic chromosome
Cytosine Methylation
- impedes transcription
- turn genes "off"
- important for transposon silencing
Transposon
- sequences of DNA that can move or transpose themselves to new positions within the genome of a single cell
Zygote
- the cell created by the union of two games, in which the gamete nuclei are also fused
- earliest stage of the diploid generations
- result of fertilization
DNA Polymerase
- any of a group of enzyme that catalyze the formation of DNA strands from a DNA template
Carl Linnaeus (1707-1778)
- father of taxonomy
- established conventions for naming of living organisms using binomial nomenclature
- developed a hierarchical system of classification of organisms
Gregor Mendel (1822-1884)
- father of modern genetics
- demonstrated that the inheritance of certain traits in pea plants follows particular patterns --> laws of Mendelian inheritance
Charles Darwin (1809-1882)
- theory of natural selection
- all life is a continuous struggle in which on the fittest can survive
- descent with modification
- Origin of Species --> theory of evolution
Watson and Crick (1953)
- described the double helix structure of DNA
- the solution to the structure of DNA achieved through model building
- structure is double-stranded, right-handed, antiparallel, and outer edges of nitrogenous bases are exposed in major and minor grooves
Beadle and Tatum
- worked to determine whether each gene determines an enzyme in a biochemical pathway
- confirmed Garrod's one-gene, one-enzyme hypothesis
- if an organisms cannot convert one particular compound to another, it lacks an enzyme required for conversion
Gene Structure
- coding region (makes structure)
- regulatory region (enhancers, promoter)
DNA Sequences Act As:
- binding sites for proteins
- a template for RNA production
- signals for RNA processing
DNA Methylation
- play major role in cancer
Promoter
- special sequence of DNA to which RNA Polymerase binds very tightly
- tells where to start transcription and which strand of DNA to transcribe
Mendelian Laws of Inheritance
- every individual possesses a pair of alleles passed down by each parent
- separate genes of separate traits are passed down independently of one another
Enhancer
- element that, upon binding with transcription factors, can enhance transcription
- transcription factors = transcriptional activators
Silencer
- element that, upon binding with transcription factors, can repress transcription.
- transcription factors = repressors
Response Element
- recognition site of certain transcription factors
Transcriptional Region
- part of DNA to be transcribed into RNA molecule
Regulatory Region
- trans-regulatory = DNA sequences that encode transcription factors
- cis-regulatory = binding sites of transcription factors that can affect transcription
Transcriptional Region
- part of DNA to be transcribed into RNA molecule
Regulatory Region
- trans-regulatory = DNA sequences that encode transcription factors
- cis-regulatory = binding sites of transcription factors that can affect transcription