BIO1110 Exam II Study Guide: Photosynthesis, Molecular Genetics, Cell Division, and Biotechnology

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Comprehensive vocabulary flashcards covering Photosynthesis, DNA replication, Transcription, Translation, Mutations, Gene regulation, the Cell Cycle, Mitosis, Meiosis, Mendelian genetics, and Biotechnology for Exam II BIO1110.

60 Terms

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Photosystem

A light-capturing unit located in the thylakoid membrane consisting of a reaction-center complex surrounded by light-harvesting complexes.

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Calvin Cycle

The light-independent reactions of photosynthesis that utilize ATP and NADPH produced by the light reactions to fix carbon dioxide into carbohydrates.

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5' and 3' Ends

The directional orientations of a nucleic acid strand determined by whether the fifth or third carbon of the ribose or deoxyribose sugar is free with an attached phosphate or hydroxyl group.

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Semiconservative DNA Replication

The mechanism of DNA replication in which each newly synthesized double helix is composed of one conserved parental template strand and one newly formed daughter strand.

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Template Strand

The specific DNA strand of the double helix that RNA polymerase reads to synthesize a complementary RNA transcript during transcription.

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Promoter

A specific sequence of DNA where RNA polymerase binds to initiate transcription.

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Primary Transcript

The initial, unedited RNA molecule synthesized directly from the DNA template strand before undergoing post-transcriptional processing in eukaryotic cells.

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RNA Processing

The eukaryotic modification of a pre-mRNA transcript, including 5' capping, 3' polyadenylation, and splicing out of introns.

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Intron

A noncoding intervening sequence within a eukaryotic pre-mRNA that is removed during RNA splicing.

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Exon

A coding region of a eukaryotic pre-mRNA transcript that remains after splicing and is expressed into an amino acid sequence.

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Codon

A three-nucleotide sequence in mRNA that codes for a specific amino acid or acts as a start or stop signal during translation.

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Transfer RNA (tRNA)

An RNA molecule that carries a specific amino acid to the ribosome and base-pairs with the complementary mRNA codon using its anticodon.

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Anticodon

A triplet of nucleotides on a tRNA molecule that base-pairs complementarily with a specific mRNA codon during translation.

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Ribosomal RNA (rRNA)

The structural and catalytic RNA component of a ribosome that facilitates the translation of mRNA into protein.

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Silent Mutation

A point mutation in DNA that changes a nucleotide without altering the amino acid sequence of the encoded protein.

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Missense Mutation

A point mutation in which a single base substitution changes a codon to specify a different amino acid.

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Nonsense Mutation

A point mutation that changes an amino-acid-coding codon into a premature stop codon, terminating polypeptide synthesis early.

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Frameshift Mutation

A mutation resulting from the insertion or deletion of nucleotides not in multiples of three, shifting the reading frame of the entire downstream sequence.

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Differential Gene Expression

The expression of distinct sets of genes by cells with identical genomes, allowing different cell types to develop specialized structures and functions.

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Epigenetics

The study of heritable changes in gene expression and cellular phenotype that do not involve alterations to the underlying DNA nucleotide sequence.

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DNA Methylation

The addition of methyl groups to DNA bases, typically resulting in chromatin condensation and the long-term repression of transcription.

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Histone Acetylation

The enzymatic addition of acetyl groups to histone tails, which loosens chromatin structure and promotes active transcription.

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G1 Phase

The first growth phase of interphase during which the cell grows in size, synthesizes proteins, and carries out metabolic tasks before DNA synthesis.

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S Phase

The synthesis phase of interphase during which the cell replicates its entire genomic DNA.

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G2 Phase

The second gap phase of interphase where the cell completes final preparations, synthesizes spindle proteins, and checks for DNA damage prior to mitosis.

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Prophase

The initial stage of mitosis during which chromatin condenses into visible chromosomes, the nucleolus disappears, and the mitotic spindle begins to assemble.

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Prometaphase

The stage of mitosis characterized by the breakdown of the nuclear envelope and the attachment of spindle microtubules to chromosomal kinetochores.

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Metaphase

The stage of mitosis where chromosomes align along the metaphase plate in the center of the dividing cell.

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Anaphase

The mitotic stage where sister chromatids separate into individual daughter chromosomes and migrate toward opposite poles of the spindle apparatus.

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Telophase

The final stage of mitosis during which daughter nuclei form at each pole, the nuclear envelope reforms, and chromosomes decondense.

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Cytokinesis

The physical division of the cytoplasm into two distinct daughter cells, occurring via a cleavage furrow in animal cells and a cell plate in plant cells.

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Proto-oncogene

A normal cellular gene that stimulates cell division and growth under strict regulation in healthy cells.

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Oncogene

A mutated, hyperactive version of a proto-oncogene that causes unchecked, excessive cell proliferation leading to cancer.

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Tumor Suppressor Gene

A gene whose normal protein product inhibits cell division, repairs damaged DNA, or initiates apoptosis, preventing tumor formation.

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Diploid (2n2n)

A cell or organism that possesses two complete sets of chromosomes, one contributed by each parent.

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Haploid (nn)

A cell containing a single set of unpaired chromosomes, typical of gametes produced by meiosis.

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Autosomes

Chromosomes that are not directly involved in determining the biological sex of an individual.

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Sex Chromosomes

Chromosomes that determine the genetic sex of an organism (such as X and Y in humans).

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Homologous Chromosomes

A pair of matching chromosomes having the same length, centromere position, and gene loci, with one inherited from each parent.

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Sister Chromatids

Two identical copies of a duplicated chromosome produced during S phase and joined together at a common centromere.

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Meiosis I

The first division of meiosis, termed reductional division, in which homologous chromosome pairs are separated.

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Meiosis II

The second division of meiosis, termed equational division, in which sister chromatids are separated.

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Crossing Over

The reciprocal exchange of genetic material between non-sister chromatids of homologous chromosomes during prophase I of meiosis.

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Independent Assortment

The random distribution of maternal and paternal homologous chromosome pairs to opposite poles during metaphase I and anaphase I of meiosis.

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Nondisjunction

An error during cell division where homologous chromosomes or sister chromatids fail to separate properly, producing aneuploid gametes or daughter cells.

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Aneuploidy

A chromosomal condition in which a cell has an abnormal number of chromosomes, such as having one extra or one missing chromosome.

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Allele

Any of the alternative versions of a gene that produce distinguishable phenotypic effects.

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Law of Segregation

Mendel's first law stating that two alleles for a heritable character segregate during gamete formation and end up in different gametes.

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Law of Independent Assortment

Mendel's second law stating that each pair of alleles segregates independently of any other pair of alleles during gamete formation.

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Incomplete Dominance

A pattern of inheritance where heterozygous individuals express a phenotype that is intermediate between the two homozygous parental phenotypes.

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Pleiotropy

The ability of a single gene to have multiple, seemingly unrelated phenotypic effects throughout an organism.

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Epistasis

A type of gene interaction in which the phenotypic expression of one gene alters or masks the phenotypic expression of a second, independently inherited gene.

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Pedigree

A standardized family tree diagram that displays the occurrence and inheritance pattern of specific traits or genetic conditions across generations.

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Recombinant DNA

A DNA molecule formed in a laboratory setting by combining genetic material from two or more distinct biological sources.

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Vector

A DNA molecule, such as a plasmid or viral genome, used to carry foreign genetic material into a host cell for cloning or expression.

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Restriction Enzyme

An endonuclease used in biotechnology that cleaves DNA molecules at specific, recognized nucleotide sequences.

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Gel Electrophoresis

A laboratory method that separates charged macromolecules like DNA fragments by size as they migrate through an electric field in an agarose gel.

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Chain Termination Sequencing Method

A DNA sequencing method that incorporates modified dideoxynucleotides lacking a 3'-OH group to halt elongation at specific base positions.

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Polymerase Chain Reaction (PCR)

An in vitro molecular technique used to rapidly amplify a specific target segment of DNA using repeated cycles of denaturation, annealing, and extension.

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CRISPR-Cas9

A gene editing system derived from bacterial immunity that employs a synthetic guide RNA and the Cas9 endonuclease to introduce precise double-stranded cuts in DNA.