Exam 1 Flashcards
(43 cards)
What is regulating gene expression and why is it important?
Regulating gene expression controls when and how specific genes are expressed. This allows for proper development of cells, organs, and systems, and adaptation to changes in the environment. It also prevents diseases and disorders such as cancer.
What is a transcription factor and how does it regulate gene expression?
A transcription factor is a protein that binds to specific DNA sequences and controls the rate of transcription of genes into RNA. This controls the amount of protein produced from a gene, affecting the phenotype of the cell or organism.
What are iPSCs?
Induced pluripotent stem cells, adult cells that have been genetically reprogrammed to an embryonic stem cell-like state with the ability to differentiate into any type of cell in the body.
What are the potential uses of iPSCs?
Treating human genetic conditions by creating patient-specific cells, and understanding genetic conditions in a more personalized manner.
What is the role of transcription factors in making iPSCs?
Transcription factors are responsible for reprogramming adult cells back to a pluripotent state by introducing specific transcription factors like Oct4, Sox2, Klf4, and c-Myc.
How are iPSCs made?
iPSCs are made by introducing specific transcription factors into adult cells, such as skin cells, via viral vectors or other methods, causing the cell’s genome to change, allowing it to become pluripotent.
What is the basic unit of life?
Cells
What are the components of a cell?
Cell membrane, cytoskeleton, cytoplasm, nucleus, mitochondria, endoplasmic reticulum (ER) and Golgi apparatus, ribosomes, lysosomes
What are the general functions of major cellular organelles?
Cell membrane: selectively permeable barrier that surrounds the cell and controls the movement of materials in and out of the cell. Cytoskeleton: network of protein fibers that provide structural support and shape to the cell. Cytoplasm: gel-like substance that fills the cell and contains all the cell’s organelles. Nucleus: contains the cell’s genetic material and controls the cell’s growth and reproduction. Mitochondria: site of cellular respiration, which generates energy for the cell. Endoplasmic reticulum (ER) and Golgi apparatus: organelles responsible for protein synthesis and processing. Ribosomes: site of protein synthesis. Lysosomes: cell organelles that contain enzymes for breaking down and recycling cellular waste products.
What is the cellular basis of disease?
Alteration of the normal functioning of cells, caused by genetic mutations, environmental factors, or infectious agents.
What are the differences between somatic cells and germ cells?
Somatic cells are any cells of the body other than the reproductive cells (germ cells). Germ cells are the reproductive cells, such as eggs and sperm, that give rise to the next generation.
What is the genetic information of an organism organized into?
The genetic information of an organism is organized into DNA molecules, which are made up of nucleotides. The DNA is organized into chromosomes, which are long, linear structures made up of DNA and proteins. The chromosomes are found in the nucleus of a cell and the complete set of chromosomes in a cell is called the genome.
What is ploidy?
Ploidy refers to the number of sets of chromosomes in a cell. Haploid cells have one set of chromosomes (n), diploid cells have two sets of chromosomes (2n), and so on. This relates to the number of homologs of each chromosome because each chromosome has a homologous partner, and the number of homologous pairs present in a cell is determined by the ploidy level.
What is the correct ploidy for human somatic cells?
The correct ploidy for human somatic cells is diploid (2n).
What is the correct ploidy for human germ cells?
The correct ploidy for human germ cells is haploid (n).
What is the relationship between phenotype and genotype?
The relationship between phenotype and genotype is that the phenotype is the observable characteristics of an organism and the genotype is the genetic makeup of an organism. Phenotype is determined by the genotype and the environment.
What is a gene?
A gene is a segment of DNA that codes for a specific trait or characteristic, such as eye color or blood type.
What is an allele?
An allele is a variant of a gene. Recessive alleles are not expressed when a dominant allele is present. Dominant alleles are always expressed, even when a recessive allele is present.
What are chromosomes?
Chromosomes are the structures in the nucleus of a cell that carry genetic information. Replicated chromosomes are identical copies of a single chromosome. Sister chromatids are the identical copies of a chromosome that are joined at a centromere. Homologous chromosomes are pairs of chromosomes that carry the same genes in the same order, but may have different versions of those genes (alleles).
What is the cell cycle?
The cell cycle is the series of events that occur in a cell leading to its division and duplication (replication). The major phases of the somatic cell cycle are: interphase (G1, S, G2) and the mitotic phase (M).
What is mitosis?
Mitosis is the process by which a single cell divides to produce two identical daughter cells. It is a continuous process that can be divided into four main stages: prophase, metaphase, anaphase, and telophase. In prophase, the chromatin condenses into visible chromosomes. In metaphase, the chromosomes line up at the center of the cell. In anaphase, the sister chromatids separate and are pulled to opposite poles of the cell. In telophase, the chromosomes reach the opposite poles of the cell and decondense back into chromatin. Mitosis is important for a number of biological processes, including cell growth and repair, tissue regeneration, and the maintenance of chromosome number during cell division.
What is the “central dogma” of genetic information transfer?
The “central dogma” is a fundamental concept in molecular biology that describes the flow of genetic information in living organisms. It states that DNA is transcribed into RNA, which is then translated into proteins, and the flow is unidirectional, meaning that information cannot flow from protein to RNA to DNA.
What is transcription?
Transcription is the process by which the genetic information stored in DNA is used to make a complementary RNA molecule. It occurs in the nucleus of a cell and involves the enzymes RNA polymerase and several other transcription factors.
What is the role of RNA processing after transcription?
After transcription, the RNA transcript goes through processing steps, including capping and polyadenylation, that modify the ends of the transcript and protect it from degradation. Also, non-coding sequences called introns are removed and the coding sequences called exons are spliced together to form a mature mRNA.