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GracefulGauss4557

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Ashley Santos, Femmela Chan, Danielia Fernandez

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menstrual cycle DNA RNA biology

Summary

This document provides a summary of the menstrual cycle, DNA, RNA, and chromosomes. It includes details about the menstrual cycle, its phases, and associated hormones, along with an overview of DNA and RNA components and functions within cells. The text also discusses different types of mutations and their effects on the body.

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SCIENCE QE REVIEWER BY: 10-AOM (ASHLEY SANTOS, FEMMELA CHAN, DANIELLA FERNANDEZ) 3 MUSKETEERS POINTERS: 1.​ Menstrual Cycle 2.​ DNA vs. RNA a.​ Complementary Base Pairings in DNA and RNA 3.​ Central Dogma of Molecular Genetics a.​...

SCIENCE QE REVIEWER BY: 10-AOM (ASHLEY SANTOS, FEMMELA CHAN, DANIELLA FERNANDEZ) 3 MUSKETEERS POINTERS: 1.​ Menstrual Cycle 2.​ DNA vs. RNA a.​ Complementary Base Pairings in DNA and RNA 3.​ Central Dogma of Molecular Genetics a.​ Protein Synthesis through: -​ Replication -​ Transcription -​ Translation 4.​ DNA Mutation a.​ Gene Mutation and Chromosomal Mutation b.​ Genetic Disorder MENSTRUAL CYCLE is the cycle of physiological changes from the beginning of one menstrual period. ​ MENSTRUATION -​ The regular discharge of blood, uterine tissues, and unfertilized egg cells. a.​ MENARCHE -​ The first on-set of menstruation. ​ DYSMENORRHEA -​ is also called Menstrual Cramps. -​ characterized by throbbing or cramping pains in the lower abdomen. -​ may occur before and during their menstrual periods. PHASES OF THE MENSTRUAL CYCLE ​ LUTEINIZING HORMONE (LH) ​ CORPUS LUTEUM -​ Responsible for releasing the -​ is made from a follicle that houses a matured egg cell in the ovary. maturing egg. -​ Aids in egg maturation. -​ A corpus luteum is a mass of cells -​ Provides the hormonal trigger to that forms in an ovary. It is a cause ovulation (release of eggs temporary organ that appears every from the ovary). menstrual cycle and disappears if fertilization does not occur. ​ WHY IS THE MENSTRUAL CYCLE SIGNIFICANT AMONG FEMALES? 1.​ REPRODUCTION -​ The cycle prepares the body for potential pregnancy by regulating ovulation, the release of an egg from the ovary. 2.​ HORMONAL REGULATION -​ It helps maintain a balance of hormones such as estrogen and progesterone, essential for various bodily functions. 3.​ HEALTH INDICATOR -​ A regular menstrual cycle is often a sign of good health, while irregularities can signal underlying medical conditions like hormonal imbalances or stress. 4.​ ENDOMETRIAL RENEWAL -​ The shedding of the uterine lining during menstruation ensures a healthy environment for embryo implantation in future cycles ​ NOTES 1.​ How many days is the regular menstrual cycle? -​ 28 days – regular menstrual cycle. 2.​ How many days is the flow of menses? -​ 3 to 7 days – the flow of menses. 3.​ On what day has the egg been released or ovulated? -​ 14th day of 28 days REGULAR cycle – ovulation or release of egg cells. 4.​ Describe the uterine wall – endometrium on days 21-28. -​ The endometrium thickens on days 21-28. 5.​ human chorionic gonadotropin (hCG) is the hormone pregnancy tests detect DNA VS RNA ​ CHROMOSOME -​ A chromosome is a packaged and organized chromatin, a complex of macromolecules found in cells, consisting of DNA and protein. > DNA - Deoxyribonucleic acid > RNA - Ribonucleic acid ​ FUNCTIONS OF A CHROMOSOME https://www.youtube.com/watch?v=d_-XWjlhLyk https://www.youtube.com/watch?v=-hryHoTIHak 1.​ It stores and transmits HEREDITARY information in the form of GENES. 2.​ Ensure accurate replication and distribution of DNA during cell division (mitosis & meiosis). ​ GENES -​ Are segments of the DNA. -​ They carry the genetic information of an organism. ​ HUMAN CHROMOSOMES -​ 23 pairs or 46 chromosomes -​ 22 pairs or 44 body chromosomes/ autosomes -​ 1 pair or 2 sex chromosomes ​ HAPLOID CHROMOSOME ​ DIPLOID CHROMOSOME -​ Unduplicated. -​ Duplicated. -​ With half the number of -​ With a complete number of chromosomes. chromosomes. -​ Contains 23 chromosomes. -​ Contains 46 chromosomes. EXAMPLE: EXAMPLE: -​ Gametes or sex cells (sperm and -​ Somatic cells or body cells (skin, RBC, egg cells). hair, bone, etc.) STRUCTURES OF THE DNA ​ PIONEERS OF THE DNA MODEL (1953) 1.​ James Watson 2.​ Francis Crick ​ NITROGEN BASES OF DNA 1.​ Adenine (A) 2.​ Cytosine (C) 3.​ Guanine (G) 4.​ Thymine (T) ​ CHARGAFF’S RULE OF DNA -​ The amount of Adenine (A) = The amount of Thymine (T) -​ The amount of Guanine (G) = The amount of Cystosine (C) ​ NITROGEN BASES OF RNA 1.​ Adenine (A) 2.​ Cytosine (C) 3.​ Uracil (U) 4.​ Guanine (G) THE CENTRAL DOGMA OF MOLECULAR GENETICS ​ DOGMA -​ A principle or set of principles. ​ REPLICATION -​ Copying or duplication of DNA before cell division. ​ TRANSCRIPTION -​ DNA is copied into messenger RNA (mRNA) in the nucleus. ​ TRANSLATION -​ mRNA is decoded by ribosomes in the cytoplasm to assemble a specific protein. ​ CODON -​ A sequence of three nucleotides in mRNA that codes for a specific amino acid. ​ NUCLEOTIDE -​ The basic unit of DNA and RNA, consists of a sugar (deoxyribose or ribose), a phosphate group, and a nitrogenous base (A, T, C, G in DNA; A, U, C, G in RNA). ​ AMINO ACID -​ building blocks of proteins. ​ PROTEIN -​ A complex molecule made of amino acids that performs various functions in the body, such as enzymes, hormones, and structural components. ​ THE CENTRAL DOGMA OF MOLECULAR GENETICS -​ Explains the flow of genetic information, from DNA to mRNA (TRANSCRIPTION), to make a functional product, a protein (TRANSLATION). -​ states that the pattern of information that occurs in our cells are: 1.​ From existing DNA to make new DNA (replication) 2.​ From DNA to make new mRNA (transcription) 3.​ From mRNA to make new proteins (translation) EXAMPLE: https://www.youtube.com/watch?v=gG7uCskUOrA DNA MUTATION -​ Di pa po nalelesson : ( -​ Thanks imacu 😀 ​ MUTATIONS -​ are changes made to an organism’s genetic material. -​ changes may be due to errors in replication, errors during transcription, radiation (exposure to mutagens), and viruses (viral infection). ​ FACTORS THAT CAUSE DNA MUTATION 1.​ RADIATION -​ UV Radiation: Both natural sunlight and tanning beds. -​ X-ray: Medical, dental, Airport security screening. 2.​ CHEMICALS -​ Cigarette Smoke: Contain dozens of mutagenic chemicals. -​ Nitrate & Nitrite Preservatives: Found in processed meats. -​ Barbecuing: Creates mutagenic chemicals in foods -​ Benzoyl Peroxide: Common ingredient in acne products. 3.​ INFECTIOUS AGENTS -​ Human Papillomavirus (HPV): Sexually transmitted virus. -​ Helicobacter pylori: Bacteria spread through contaminated food. ​ TYPES OF MUTATIONS 1.​ GENE MUTATION - GENE ALTERATION -​ A change in one or more genes can lead to genetic disorders or illness. 2.​ CHROMOSOMAL MUTATION - CHROMOSOMAL ABNORMALITY -​ Changes to the structure or number of chromosomes. ​ FIVE TYPES OF CHROMOSOMAL MUTATIONS ​ POINT MUTATIONS -​ Large category of mutations that describe a change in a single nucleotide of DNA, that causes that DNA to be different from the normal type of gene sequence. 1.​ INSERTION -​ Extra base pair is added to a sequence of bases. a.​ BETA-THALASSEMIA -​ Blood disorder that reduces the production of hemoglobin. 2.​ DELETION -​ Extra base pair is deleted from a sequence. -​ Loss of a part. -​ Loss of large regions of a chromosome. a.​ CYSTIC FIBROSIS -​ Hereditary disease that affects the lungs and digestive system. -​ The body produces a thick and sticky mucus that can clog the lungs and obstruct the pancreas. 3.​ DUPLICATION -​ Extra copies of a sequence. -​ Duplication of a few bases. 4.​ INVERSION -​ The order of genes in the chromosomes is inverted 5.​ TRANSLOCATION -​ Part of one chromosome is transferred to another chromosome.\ ​ GENETIC DISORDER -​ Caused by DNA mutations. -​ Heritable or inheritable. ​ EXAMPLES OF GENETIC DISORDER 1.​ TAY-SACHS DISEASE -​ Recessive gender disorder. -​ Abnormal accumulation of GM2 (fatty substance) -​ Defect in HEXA gene (hexosaminidase)? -​ Muscle weakness. -​ Speech problems. -​ Impaired cognitive and motor functions. a.​ HEXASAMINIDASE-A -​ Brain and spinal cord. -​ Enzymes found at lysosomes. -​ Break down toxic substances and act as recycling centers. 2.​ SICKLE CELL ANEMIA (SCA) -​ Single gene disorder -​ Hemoglobin gene -​ Chromosome 11 -​ Hydrophobic amino acid (valine) replaces hydrophilic acid -​ Red blood cells become sickle -​ Pain in arms, legs, chest and abdomen -​ Recurrent infections 3.​ PHENYLKETONURIA (PKU) -​ Protein phenylalanine hydroxylase (PAH) -​ Phenylalanine to tyrosine -​ Normal at birth -​ Stunted growth -​ Epilepsy -​ Behavioral problems -​ Skin rash -​ Mouse-like body odor 4.​ HEMOPHILIA -​ Impaired blood-clotting ability -​ Bleed longer -​ Bleed internally 5.​ CRI-DU-CHAT SYNDROME -​ Cat’s cry syndrome -​ Chromosome 5 is missing -​ Low birth and poor growth -​ Severe cognitive, speech, and motor delays -​ Behavioral problems (tantrums, hyperacidity, motor delays) 6.​ DOWN SYNDROME -​ Trisomy 21 -​ Mild to serious physical and developmental problems -​ Congenital cardiac -​ Gastrointestinal anomalies -​ Autoimmune conditions -​ Respiratory infections -​ Sleep disorders -​ Hearing and vision loss 7.​ EDWARD’S SYNDROME -​ Trisomy 18 -​ Babies born with the condition usually do not survive for much longer than a week

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