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Premedical- Biology Meiosis 1.

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Presentation on theme: "Premedical- Biology Meiosis 1."— Presentation transcript:

1 Premedical- Biology Meiosis 1

2 Reproduction The ability to produce new individual organisms,
either asexually from a single parent organism, or sexually from two parent organisms. Asexual reproduction is not limited to single-celled organisms - most plants - binary fission- Bacteria - budding - yeasts and Hydras - conjugation - bacteria may exchange genetic information parthogenesis, fragmentation and spore formation 2

3 Parthenogenesis lower plants (where it is called apomixis)
Aphis Aphid Green-fly Wingless female giving birth baby hammerhead Parthenogenesis lower plants (where it is called apomixis) invertebrates - water fleas, aphids, some bees and parasitic wasps vertebrates - some reptiles, fish, and very rarely birds and sharks Water flea = dafhnia Perloočky, Cladocera Cladocerans, water fleas Zástupci korýšů Crustacea podtřídy Phyllopoda řádu Cladocera. and development of embryo or seed without fertilization by a male 3

4 male produce sperm or microspore in anisogamous species
Sexual reproduction by combination of genetic material contributed from two different members of the species Each contributes half of the offspring's genetic material male produce sperm or microspore in anisogamous species and female produce ovum or megaspore Most organisms form two different types of gametes. For example, in the green alga, Chlamydomonas reinhardtii, there are so-called "plus" and "minus" gametes. Most animals (including humans) and plants reproduce sexually. 4

5 called alleles, offspring inherit one allele from each parent
Sexually reproducing organisms have two sets of genes for every trait called alleles, offspring inherit one allele from each parent offspring is combination of parental genes diploid and haploid phases alternation in cell lines inbreeding = reproduction from mating of two genetically related parents inbred line – genesis of homozygote offsprings by sexual reproduction 5

6 Human reproduction cycle Lenght, duration

7 Meiosis = division of germ cells - reduction of diploid chromosomal number to haploid - formation of haploid gametes To manage the most number of various alleles of genes.

8 First meiotic division
M I = reduction 2n = heterotypic Prophase I: leptotene – spiralisation of chromosomes zygotene – pairing of homologous chromosomes – synapsis - bivalents synaptonemal complex 8

9 = three levels of protein structure
Synaptonemal komplex = three levels of protein structure

10 3. pachytene – each chromosome has two chromatids – tetrades
crossing-over = reciprocal exchange of homologous parts of non-sister chromatids = recombination of maternal and paternal genetic material Recombination possibilities between non-sister chromatids and result products- two chiasmata on one bivalent a - recombination only between 2 chromatids; b - 4 chromatids in recombination; c - 3 chromatids in recombination. 10

11 prerequisite of crossing-over = chiasma formation
4. diplotene – separation of homologs, connected only in sites of chiasmata. prerequisite of crossing-over = chiasma formation 5. diakinesis – terminalisation of chiasmata and maximal contraction of chromosomes Metaphase I – lining of bivalents in equatorial plane of the cell. Chromosomes from the pairs split. 11

12 spermiogenesis, unequal in oogenesis
Anaphase I – migration of homologous chromosomes to the opposite poles - random according to their parental origin Telophase I - chromosomes in opposite poles Cytokinesis – division of cytoplasm - equal in spermiogenesis, unequal in oogenesis Interkinesis – a phase without replication

13 Second meiotic division
M II – homeotypic n in Prophase II division and separation of centriols – spindle of microtubules in Metaphase II centromers of chromosomes split in Anaphase II separation of chromatids 13

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16 Gametogenesis migration of primordial germ cells to the gonads
– formation of gametes migration of primordial germ cells to the gonads during early fetal development number of mitotic division

17 Spermatogenesis is continuous process, which starts in the time of sexual maturity (top off testosteron threshold) growth MI mitotic division - spermatogonia primary spermatocyte (dipl) M II 2 secondary spermatocytes (hapl) spermatids diferentiation-spermiogenesis 4 sperm 1 cycle = about 10 weeks 17

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19 3 month of fetal life diplotene=dictyotene growth at the time of birth
Oogenesis M I to the end of prophase 3 month of fetal life diplotene=dictyotene growth at the time of birth Oogonia primary oocyte (dipl) mitotic division in the time of sexual maturity M II M I continues secondary oocyte ovulation in metaphase II st polar body anaphase II + telophase II only after fertilization oocyte + 2nd polar body 19

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21 Oogenesis prenatal oogonia Mitotic division growth M I meiosis M II
primary oocyte secondary oocyte growth M I M II meiosis 1st polar body 2nd polar body 3rd month of fetal life - Dictyotene MI division stops at time of birth Sexual maturity- Metaphase MII - ovulation Fertilization – pronucleus Ovum after MII pronucleus Anaphase II, Telophase II only after fertilization prenatal zygote egg cell Sexual maturity Oogenesis 21

22 Oogenesis a fertilization
I. meiotic division polar body oogonia primary secondary oocyte n 2n fertilization a II. Meiotic division

23 23

24 Differences in gametogenesis Male Female
Initiation Puberty Early embryonic life Duration cca 72 days years Numbers of mitoses in gamete formation Gamete production spermatids ovum+3 polar bodies Gamete production million ovum per menstrual per ejaculate cycle 24

25 Degeneration of germ cells in ovary
5th month of fetal life x of cells time of birth x of cells puberty of cells ovulated of cells Long period between M I and ovulation = factor of high probability of nondisjunction 25

26 Consequences of meiosis
reduction of diploid chromosomal number to haploid segregation of alleles in M I, M II (2st Mendel´s law) 3. random assortment of homologues – random combination maternal and paternal chromosomes in gametes (3nd Mendel´s law) 4. increase of genetic variability by crossing-over (chromatids with segments of maternal and paternal origin) 26

27 Genetic determination of sex
23,Y 27

28 If you feel small, low-spirited and useless, remember:
Thanks to the perfect Ovum and the fastest Sperm and their genetic information, YOU ARE ABSOLUTELY UNIQUE and NOT REPEATABLE ELEMENT IN THE WHOLE UNIVERSE

29 Thank you for your attention
Campbell, Neil A., Reece, Jane B., Cain Michael L., Jackson, Robert B., Minorsky, Peter V., Biology, Benjamin-Cummings Publishing Company, 1996 –2010.

30 Repetition 7. Regulation of gene expression
1. What is the difference between prokaryotic and eukaryotic regulation of gene expression? 2. What is operon and how does it work? Example? 3. Which steps on the path between eukaryotic gene and protein can be regulated? 4. What does it mean „imprinting“? 5. What is the purpose if acetylation and deacetylation of histones? 6. What is the function of transcription factors? 7. What is alternative splicing? 8. Do you know any post-translational modifications? 9. How are proteins degradated? 10. What is the „central dogma“ of biology? (path of genetic information)


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