Meiosis Meiosis

Total Page:16

File Type:pdf, Size:1020Kb

Meiosis Meiosis MEIOSIS MEIOSIS KEY CONCEPT Gametes have half the number of chromosomes that body cells have. MEIOSIS : CELL TYPES You have Body cells and Gametes Body cells are also called somatic cells. Germ cells develop into gametes. Germ cells are located in the ovaries and testes. Gametes are sex cells: egg and sperm. Gametes have DNA that can be passed to offspring. MEIOSIS : ALL ABOUT CHROMOSOMES Your cells have autosomes & sex chromosomes • Your body cells have 23 pairs of chromosomes. – Homologous pairs of chromosomes have the same structure and genetic material. – For each homologous pair, one chromosome comes from each parent. • Chromosome pairs 1-22 are autosomes. • Sex chromosomes, X and Y, determine gender in mammals. MEIOSIS : DIPLOID AND HAPLOID Diploid (2n) cells have two copies of every chromosome. Body cells are diploid. Half the chromosomes come from each parent. In humans this means we have 2 sets of 23 chromosomes (total of 46) MEIOSIS : DIPLOID AND HAPLOID Haploid (n) cells have one copy of every chromosome. – Gametes are haploid. – In humans gametes have 22 autosomes and 1 sex chromosome. (23 total) MITOSIS REVIEW Goal of Mitosis is Chromosome number must be maintained. • Mitosis and meiosis are types of nuclear division that make different types of cells with different number of chromosomes. • Mitosis makes more diploid cells. • Number of Chromosomes in parent is Equal to the number of chromosomes in offspring. INTRODUCTION TO MEIOSIS Meiosis makes haploid cells from diploid cells. This happens because cells go through TWO rounds of division during meiosis. Meiosis reduces chromosome number and creates genetic diversity. Meiosis Occurs in Sex cells Meiosis Produces gametes. MEIOSIS DETAIL KEY CONCEPT During meiosis, diploid cells undergo two cell divisions that result in haploid cells. homologous chromosomes Meiosis I and Meiosis II Meiosis I and meiosis II each have four phases, similar to those in mitosis. Biggest difference is the how the DNA organizes for each division. In Meiosis I Pairs of homologous chromosomes form tetrads. sister sister chromatids chromatids MEIOSIS DETAIL KEY CONCEPT During meiosis, diploid cells undergo two cell divisions that result in haploid cells. Meiosis I pairs of homologous chromosomes (tetrads) separate. Homologous chromosomes are similar but not identical genetically In Meiosis II SISTER CHROMATIDS separate. MEIOSIS I DETAILS • Meiosis I occurs after DNA has been replicated. • Meiosis I divides homologous chromosomes in four phases. Prophase I Metaphase I Anaphase I Telophase I PROPHASE I Each chromosome pairs with its corresponding homologous chromosome to form a tetrad. There are 4 chromosomes in a tetrad. The pairing of homologous chromosomes is the key to understanding meiosis. Crossing-over may occur here Crossing-over is when chromosomes overlap and exchange portions of their chromatids. CROSSING OVER !!!!! They do the genetic TANGO! PROPHASE I (PICTURE) Homologous Chromosomes (called Tetrads) are held together by a synapse METAPHASE I Tetrads line up along the equator Spindle fibers attach to the centromeres of each chromosome in the tetrad. ANAPHASE I The cell begins lengthening. The spindle fibers pull the homologous chromosomes apart and toward opposite ends of the cell. Sister chromatids attached at centromeres move together Disjunction Occurs – process of separation There are ½ as many chromosomes as in the original cell but the chromosome is double stranded. TELOPHASE I Movement of homologous chromosomes continues until there is a haploid set at each pole Each chromosome = linked sister chromatids At each pole, now, there is a complete haploid set of chromosomes (but each chromosome still has two sister chromatids). Nuclear membranes reforms. A cleavage furrow appears. The cell separates into 2 daughter cells. TELOPHASE I IMPORTANT NOTE IN BETWEEN MEIOSIS I and MEIOSIS II there is no INTERPHASE!!!! PROPHASE II • Meiosis I results in two haploid (N) cells. • Each cell has half the number of chromosomes as the original cell. • Spindle Reforms • Sister Chromatids are present METAPHASE II The Sister Chromatids line up .along the equator (middle) of the cell similar to metaphase in mitosis ANAPHASE II Sister chromatids separate and move to opposite ends of the cell. TELOPHASE II • Nuclear membranes form around each set of chromosomes at opposite ends of the cell • Spindle fibers break apart • Cell undergoes cytokinesis • End result is four HAPLOID cells with genetically unique information. COMPARE AND CONTRAST • Meiosis differs from mitosis in significant ways. – Meiosis has two cell divisions while mitosis has one. – In mitosis, homologous chromosomes never pair up. – Meiosis results in haploid cells; mitosis results in diploid cells. GAMETOGENESIS Haploid cells develop into mature gametes. • Gametogenesis is the production of gametes. • Gametogenesis differs between females and males. In Males: SPERMATOGENESIS – Sperm become streamlined and motile. – Sperm primarily contribute half of the DNA to an embryo. GAMETOGENESIS In Females: Oogenesis – Eggs contribute half of DNA, all of the cytoplasm, and all organelles to an embryo. – During meiosis, the egg gets most of the contents; the other cells form polar bodies. – So only one functional gamete per cycle of meiosis .
Recommended publications
  • Meiotic Prophase Abnormalities and Metaphase Cell Death in MLH1-Deficient Mouse Spermatocytes: Insights Into Regulation of Spermatogenic Progress
    Developmental Biology 249, 85–95 (2002) doi:10.1006/dbio.2002.0708 Meiotic Prophase Abnormalities and Metaphase Cell Death in MLH1-Deficient Mouse Spermatocytes: Insights into Regulation of Spermatogenic Progress Shannon Eaker,1 John Cobb,2 April Pyle, and Mary Ann Handel3 Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee 37996 The MLH1 protein is required for normal meiosis in mice and its absence leads to failure in maintenance of pairing between bivalent chromosomes, abnormal meiotic division, and ensuing sterility in both sexes. In this study, we investigated whether failure to develop foci of MLH1 protein on chromosomes in prophase would lead to elimination of prophase spermatocytes, and, if not, whether univalent chromosomes could align normally on the meiotic spindle and whether metaphase spermatocytes would be delayed and/or eliminated. In spite of the absence of MLH1 foci, no apoptosis of spermatocytes in prophase was detected. In fact, chromosomes of pachytene spermatocytes from Mlh1؊/؊ mice were competent to condense metaphase chromosomes, both in vivo and in vitro. Most condensed chromosomes were univalents with spatially distinct FISH signals. Typical metaphase events, such as synaptonemal complex breakdown and the phosphorylation of Ser10 on histone H3, occurred in Mlh1؊/؊ spermatocytes, suggesting that there is no inhibition of onset of meiotic metaphase in the face of massive chromosomal abnormalities. However, the condensed univalent chromosomes did not align correctly onto the spindle apparatus in the majority of Mlh1؊/؊ spermatocytes. Most meiotic metaphase spermatocytes were characterized with bipolar spindles, but chromosomes radiated away from the microtubule-organizing centers in a prometaphase-like pattern rather than achieving a bipolar orientation.
    [Show full text]
  • Keystone Review Module B BIO.B.1.1 – Describe the Three Stages of the Cell Cycle: Interphase, Nuclear Division, Cytokinesis
    Keystone Review Module B BIO.B.1.1 – Describe the three stages of the cell cycle: interphase, nuclear division, cytokinesis. ● Describe the events that occur during the cell cycle: interphase, nuclear division, and cytokinesis. ● Compare the processes and outcomes of mitotic and meiotic nuclear division. Which statement BEST describes the phase of the cell cycle shown? A. The cell is in prophase of mitosis because the number of chromosomes has doubled. B. The cell is in prophase I of meiosis because of the number of chromosomes has doubled. C. The cell is in telophase of mitosis because the cell is separating and contains two copies of each chromosome. D. The cell is in telophase of meiosis because the cell is separating and contains two copies of each chromosome. Answer - C A. Incorrect - The cell is not in prophase. This is obvious as the cell contains two nuclei, a condition which only occurs in telophase. B. Incorrect - The cell is not in prophase. This is obvious as the cell contains two nuclei, a condition which only occurs in telophase. C. Correct - The cell is in telophase, which can be seen from the two nuclei. Only telophase of mitosis includes two copies of each chromosome. D. Incorrect - The cell is in telophase, but in meiosis each cell contains only 1 copy of each chromosome. Mitosis and meiosis are processes by which animal and plant cells divide. Which statement best describes a difference between mitosis and meiosis? A. Meiosis is a multi-step process. B. Mitosis occurs only in eukaryotic cells. C. Meiosis is used in the repair of an organism.
    [Show full text]
  • Clinical Genetics: Mitochondrial Replacement Techniques Under the Spotlight
    RESEARCH HIGHLIGHTS Nature Reviews Genetics | AOP, published online 1 July 2014; doi:10.1038/nrg3784 BRAND X PICTURES CLINICAL GENETICS Mitochondrial replacement techniques under the spotlight Mutations in the mitochondrial genome have and quantitative PCR showed that PBs contain been associated with diverse forms of human dis- fewer mitochondria than pronuclei in zygotes and ease, such as Leber’s hereditary optic neuropathy than spindle–chromosome complexes in oocytes. and Leigh’s syndrome, a neurometabolic disorder. The researchers then evaluated the feasibility A preclinical mouse model now demonstrates the of PB1 or PB2 transfer in mice and compared feasibility of using polar body (PB) genomes as their efficacies with that of MST or PNT. Genetic donor genomes in a new type of mitochondrial analysis showed that oocytes generated by PB1 replacement technique aimed at preventing the genome transfer were fertilized at rates that are inheritance of mitochondrial diseases. comparable to those obtained for oocytes ferti- 2014 has seen a surge in interest from both lized after MST (89.5% and 87.5%, respectively). the UK Human Fertilisation and Embryology Moreover, 87.5% of PB1–oocytes and 85.7% Authority (HFEA) and the US Food and Drug of MST–oocytes developed into blastocysts. Administration (FDA) in evaluating methods By contrast, PNT–embryos developed into designed to prevent the transmission of mito- blastocysts more frequently than PB2–oocytes chondrial diseases. One approach that is currently (81.3% and 55.5%, respectively), despite similar under investigation is mitochondrial replacement cleavage rates. by pronuclear transfer (PNT), in which the paren- Normal live progeny were obtained with all of tal pronuclei of a fertilized egg containing the these techniques at birth rates similar to those mother’s mutated mitochondrial DNA (mtDNA) of an intact control group.
    [Show full text]
  • Human Reproductive Systems Males Vs. Females Learning Goals • Students Will Describe the Basic Anatomy and Physiology of the Male and Female Reproductive Systems
    Human Reproductive Systems Males vs. Females Learning Goals • Students will describe the basic anatomy and physiology of the male and female reproductive systems. Gonads are sex organs that create gametes? & excrete sex hormones Gonads are sex organs that create gametes & excrete sex hormones Male gonads are called testes Female gonads are called ovaries -Are the site of sperm production -Are the site of egg production & maturation Gametes are also called sex ?cells, and are used to create offspring with a mixture of genetic information. Gametes are also called sex cells, and are used to create offspring with a mixture of genetic information. Male gametes are called sperm Female gametes are called -produce 300-500 million per 5ml eggs/ova of semen -70,000-100,000 at birth -release 1-2 per month from puberty to menopause. Sex Hormones are chemical? signals that tell the sex organs how to function. Sex Hormones are chemical signals that tell the sex organs how to function. Male hormone is called Female hormones are estrogen testosterone and progesterone -released from the testes -released from the ovary -controls sperm production -controls egg production & release Duct systems help deliver gametes from gonads and are the site of fertilization in females and delivers sperm out of the body in males. Male duct systems include: Epididymis -site of sperm maturation (about 20 days for sperm to mature) Male duct systems include: Vas deferens -Tube for sperm to travel through as they leave the testes Male duct systems include: Urethra -shared tube for release of semen from reproductive tract and urine from the bladder.
    [Show full text]
  • Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho
    Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho To cite this version: James Umen, Susana Coelho. Algal Sex Determination and the Evolution of Anisogamy. Annual Review of Microbiology, Annual Reviews, 2019, 73 (1), 10.1146/annurev-micro-020518-120011. hal- 02187088 HAL Id: hal-02187088 https://hal.sorbonne-universite.fr/hal-02187088 Submitted on 17 Jul 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Annu. Rev. Microbiol. 2019. 73:X–X https://doi.org/10.1146/annurev-micro-020518-120011 Copyright © 2019 by Annual Reviews. All rights reserved Umen • Coelho www.annualreviews.org • Algal Sexes and Mating Systems Algal Sex Determination and the Evolution of Anisogamy James Umen1 and Susana Coelho2 1Donald Danforth Plant Science Center, St. Louis, Missouri 63132, USA; email: [email protected] 2Sorbonne Université, UPMC Université Paris 06, CNRS, Algal Genetics Group, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, CS 90074, F-29688, Roscoff, France [**AU: Please write the entire affiliation in French or write it all in English, rather than a combination of English and French**] ; email: [email protected] Abstract Algae are photosynthetic eukaryotes whose taxonomic breadth covers a range of life histories, degrees of cellular and developmental complexity, and diverse patterns of sexual reproduction.
    [Show full text]
  • Meiosis & Sexual Reproduction Heyer 1
    Meiosis & Sexual Reproduction Meiosis & Sex Cells Arise From Preexisting Cells I. Asexual (Mitotic) Reproduction a. Mitosis: production of two identical nuclei b. Cytokinesis: physical division of the cell into two II. Sexual (Meiotic) Reproduction a. Meiosis: production of four non-identical nuclei b. Cytokinesis: physical division of the cell c. Fertilization: fusion of two Sexual reproduction creates sex cells d. Syngamy: fusion of new combinations of alleles. two nuclei Diploid cells have Homologous chromosomes [Homologs]: homologous pairs of chromosomes: same loci, maybe different alleles. 1 set from mom, 1 set from dad. Meiosis: Reductive Division Sex = Meiosis + Syngamy — Reduces Chromosome Number in Half Meiosis has 2 consecutive divisions – Meiosis I: Homologous pairs separate – Meiosis II: Sister chromatids separate Each division has a prophase, metaphase, anaphase and a telophase Meiosis: Syngamy: 2n 1n 1n 2n Diploid haploid Haploid diploid Heyer 1 Meiosis & Sexual Reproduction Chromosomes Matched in Sexual Life Cycles Homologous Pairs (Homologs) Human somatic (body) cells – 23 pairs = 46 chromosomes – Homolog = same size, shape, centromere, and genes Pairs #1 - 22 = Autosomes – Both male and female Pair #23 = Sex Chromosomes – Determine gender – XX = female, XY = male Diploid life history Alternation of Generations Haploid life history (animals) (plants) (fungi) Human karyotype Somatic (body) cells are Diploid Meiosis I Gametes (sex cells) are Haploid Diploid (2n) Prophase I – Two of each kind of chromosome Chromosomes
    [Show full text]
  • Proper Division Plane Orientation and Mitotic Progression Together Allow Normal Growth of Maize
    Proper division plane orientation and mitotic progression together allow normal growth of maize Pablo Martineza,b, Anding Luoc, Anne Sylvesterc, and Carolyn G. Rasmussena,1 aDepartment of Botany and Plant Sciences, Center for Plant Cell Biology, University of California, Riverside, CA 92521; bBiochemistry and Molecular Biology Graduate Program, University of California, Riverside, CA 92521; and cDepartment of Molecular Biology, University of Wyoming, Laramie, WY 82071 Edited by Elliot M. Meyerowitz, Howard Hughes Medical Institute and California Institute of Technology, Pasadena, CA, and approved January 17, 2017 (received for review November 23, 2016) How growth, microtubule dynamics, and cell-cycle progression are dynamics during mitosis. Similar to mutants with defects in both coordinated is one of the unsolved mysteries of cell biology. A interphase and mitotic microtubule dynamics, maize tan1 mu- maize mutant, tangled1, with known defects in growth and proper tants have short stature and misoriented cell patterns (23), as do division plane orientation, and a recently characterized cell-cycle mutants of TAN1-interacting partners phragmoplast orienting delay identified by time-lapse imaging, was used to clarify the re- kinesin-1;2 (24). TAN1 is similar to the microtubule binding lationship between growth, cell cycle, and proper division plane domain of adenomapolyposis coli (22), a multifunctional protein orientation. The tangled1 mutant was fully rescued by introduction that promotes proper division orientation in animal cells (25–27). of cortical division site localized TANGLED1-YFP. A CYCLIN1B de- In Arabidopsis thaliana, AtTAN1 fused to yellow fluorescent struction box was fused to TANGLED1-YFP to generate a line that protein (YFP) was the first identified positive marker of the cor- mostly rescued the division plane defect but still showed cell-cycle tical division site, remaining at the site after PPB disassembly (20).
    [Show full text]
  • The Diversity of Plant Sex Chromosomes Highlighted Through Advances in Genome Sequencing
    G C A T T A C G G C A T genes Review The Diversity of Plant Sex Chromosomes Highlighted through Advances in Genome Sequencing Sarah Carey 1,2 , Qingyi Yu 3,* and Alex Harkess 1,2,* 1 Department of Crop, Soil, and Environmental Sciences, Auburn University, Auburn, AL 36849, USA; [email protected] 2 HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA 3 Texas A&M AgriLife Research, Texas A&M University System, Dallas, TX 75252, USA * Correspondence: [email protected] (Q.Y.); [email protected] (A.H.) Abstract: For centuries, scientists have been intrigued by the origin of dioecy in plants, characterizing sex-specific development, uncovering cytological differences between the sexes, and developing theoretical models. Through the invention and continued improvements in genomic technologies, we have truly begun to unlock the genetic basis of dioecy in many species. Here we broadly review the advances in research on dioecy and sex chromosomes. We start by first discussing the early works that built the foundation for current studies and the advances in genome sequencing that have facilitated more-recent findings. We next discuss the analyses of sex chromosomes and sex-determination genes uncovered by genome sequencing. We synthesize these results to find some patterns are emerging, such as the role of duplications, the involvement of hormones in sex-determination, and support for the two-locus model for the origin of dioecy. Though across systems, there are also many novel insights into how sex chromosomes evolve, including different sex-determining genes and routes to suppressed recombination. We propose the future of research in plant sex chromosomes should involve interdisciplinary approaches, combining cutting-edge technologies with the classics Citation: Carey, S.; Yu, Q.; to unravel the patterns that can be found across the hundreds of independent origins.
    [Show full text]
  • Section 6: Sex Cells and Fertilisation
    S ection 6: S ex Cells and Fertilisation U se the w ords in the w ord bank below to com plete the sentences below : S maller, vagina, anther, halved, fertilisation, nucleus, male, half, gametes, D N A , stigma, female, ovules, pollen, pollen tube, four, zygote, threadlike, one, identical, genes, amino acids, protein, function, meiosis, sex chromosomes, male S ome plants reproduce sexually. T he sexual parts are inside the flow ers. M ost flow ering plants have flow ers w ith both __ ___ __ and _ ___ __ parts. T hese sexual parts produce special sex cells called _ ____ ___ _. Label the diagram above. T he male part of a flow ering plant is called the ___ ___ ___ _ and produces __ ______. T he female part is called the _ ___ ___ _ and produces ovules. Pollen grains are __ ___ ____ and more numerous than ovules, w hich are larger. Fertilisation in flow ering plants occurs by pollen trains being transferred to the _ ___ ___ _. A _____ ___ __ _____then grow s dow n into the ovary and into an ovule. A male gamete then passes dow n the tube and fuses w ith egg cell. T his process is called 1 __ __________. T he fertilised egg is now called a ___ ___ __. Fertilisation produces variety in the offspring because genetically identical gametes form in different w ays, producing different combinations. S exual Reproduction In H umans Label the follow ing diagrams: 2 In humans, fertilisation takes place in the oviduct.
    [Show full text]
  • Mitosis Vs. Meiosis
    Mitosis vs. Meiosis In order for organisms to continue growing and/or replace cells that are dead or beyond repair, cells must replicate, or make identical copies of themselves. In order to do this and maintain the proper number of chromosomes, the cells of eukaryotes must undergo mitosis to divide up their DNA. The dividing of the DNA ensures that both the “old” cell (parent cell) and the “new” cells (daughter cells) have the same genetic makeup and both will be diploid, or containing the same number of chromosomes as the parent cell. For reproduction of an organism to occur, the original parent cell will undergo Meiosis to create 4 new daughter cells with a slightly different genetic makeup in order to ensure genetic diversity when fertilization occurs. The four daughter cells will be haploid, or containing half the number of chromosomes as the parent cell. The difference between the two processes is that mitosis occurs in non-reproductive cells, or somatic cells, and meiosis occurs in the cells that participate in sexual reproduction, or germ cells. The Somatic Cell Cycle (Mitosis) The somatic cell cycle consists of 3 phases: interphase, m phase, and cytokinesis. 1. Interphase: Interphase is considered the non-dividing phase of the cell cycle. It is not a part of the actual process of mitosis, but it readies the cell for mitosis. It is made up of 3 sub-phases: • G1 Phase: In G1, the cell is growing. In most organisms, the majority of the cell’s life span is spent in G1. • S Phase: In each human somatic cell, there are 23 pairs of chromosomes; one chromosome comes from the mother and one comes from the father.
    [Show full text]
  • The Involvement of Ubiquitination Machinery in Cell Cycle Regulation and Cancer Progression
    International Journal of Molecular Sciences Review The Involvement of Ubiquitination Machinery in Cell Cycle Regulation and Cancer Progression Tingting Zou and Zhenghong Lin * School of Life Sciences, Chongqing University, Chongqing 401331, China; [email protected] * Correspondence: [email protected] Abstract: The cell cycle is a collection of events by which cellular components such as genetic materials and cytoplasmic components are accurately divided into two daughter cells. The cell cycle transition is primarily driven by the activation of cyclin-dependent kinases (CDKs), which activities are regulated by the ubiquitin-mediated proteolysis of key regulators such as cyclins, CDK inhibitors (CKIs), other kinases and phosphatases. Thus, the ubiquitin-proteasome system (UPS) plays a pivotal role in the regulation of the cell cycle progression via recognition, interaction, and ubiquitination or deubiquitination of key proteins. The illegitimate degradation of tumor suppressor or abnormally high accumulation of oncoproteins often results in deregulation of cell proliferation, genomic instability, and cancer occurrence. In this review, we demonstrate the diversity and complexity of the regulation of UPS machinery of the cell cycle. A profound understanding of the ubiquitination machinery will provide new insights into the regulation of the cell cycle transition, cancer treatment, and the development of anti-cancer drugs. Keywords: cell cycle regulation; CDKs; cyclins; CKIs; UPS; E3 ubiquitin ligases; Deubiquitinases (DUBs) Citation: Zou, T.; Lin, Z. The Involvement of Ubiquitination Machinery in Cell Cycle Regulation and Cancer Progression. 1. Introduction Int. J. Mol. Sci. 2021, 22, 5754. https://doi.org/10.3390/ijms22115754 The cell cycle is a ubiquitous, complex, and highly regulated process that is involved in the sequential events during which a cell duplicates its genetic materials, grows, and di- Academic Editors: Kwang-Hyun Bae vides into two daughter cells.
    [Show full text]
  • Cell Division- Ch 5
    Cell Division- Mitosis and Meiosis When do cells divide? Cell size . One of most important factors affecting size of the cell is size of cell membrane . Cell must remain relatively small to survive (why?) – Cell membrane has to be big enough to take in nutrients and eliminate wastes – As cells get bigger, the volume increases faster than the surface area – Small cells have a larger surface area to volume ratio than larger cells to help with nutrient intake and waste elimination . When a cell reaches its max size, the nucleus starts cell division: called MITOSIS or MEIOSIS Mitosis . General Information – Occurs in somatic (body) cells ONLY!! – Nickname: called “normal” cell division – Produces somatic cells only . Background Info – Starts with somatic cell in DIPLOID (2n) state . Cell contains homologous chromosomes- chromosomes that control the same traits but not necessarily in the same way . 1 set from mom and 1 set from dad – Ends in diploid (2n) state as SOMATIC cells – Goes through one set of divisions – Start with 1 cell and end with 2 cells Mitosis (cont.) . Accounts for three essential life processes – Growth . Result of cell producing new cells . Develop specialized shapes/functions in a process called differentiation . Rate of cell division controlled by GH (Growth Hormone) which is produced in the pituitary gland . Ex. Nerve cell, intestinal cell, etc. – Repair . Cell regenerates at the site of injury . Ex. Skin (replaced every 28 days), blood vessels, bone Mitosis (cont.) – Reproduction . Asexual – Offspring produced by only one parent – Produce offspring that are genetically identical – MITOSIS – Ex. Bacteria, fungi, certain plants and animals .
    [Show full text]