Prokaryote vs. Eukaryote Chromosomes

Slides:



Advertisements
Similar presentations
Karyotypes IB1 Biology Song Hee Bae. Karyotypes Karyotype: the number and appearance of the chromosomes in an organism. Karyotype is always found in a.
Advertisements

4.2: Meiosis ★State that meiosis is a reduction division of a diploid nucleus to form haploid nuclei. ★Define homologous chromosomes. ★Outline the process.
Chromosome disorders.
Human chromosomes There are 46 chromosomes (23 homologous pairs) in each somatic cell 22 pairs of autosomes 1 pair of sex chromosomes XX = Female, XY =
Notes: Karyotypes s.
 Mistakes made during meiosis can lead to abnormal numbers of chromosomes.  This occurs when a homologous pair of chromosomes fail to separate.  These.
Meiosis Sex Cell Formation.
Changes in Chromosome Number
Chromosomes & Human Heredity
Human Genetics – Studying Chromosomes & Diseases Biology.
Non-disjunction, Down’s syndrome, and karyotypes IB Topic 4.2.
11.3 CHROMOSOMES & HUMAN HEREDITY
KARYOTYPE Refers to the chromosome complement of a cell or a whole organism In particular, it shows the number, size, and shape of the chromosomes as seen.
Meiosis. Reproduction Asexual Asexual Results from cell division (mitosis). Results from cell division (mitosis). One “parent” cell divides to form two.
Meiosis (3.3) IB Diploma Biology Essential Idea: Meiosis produces genetically-varied, haploid cells needed for sexual reproduction.
Topic 4.2: Meiosis.
Chromosomal Abnormalities. Can occur during meiosis: During the S phase of cell cycle – mistakes in making sister chromatids. During prophase 1 – when.
Karyotypes. I. What is a Karyotype? Karyotype = a test to identify and evaluate the size, shape, and number of chromosomes in a sample of body cells.
Karyotyping. Karyotypes Chromosomes are distinguished by their appearance –size –position of centromere –pattern of bands (when stained) Karyotypes show.
Cell Division Meiosis Cell Division Meiosis Abnormal Meiosis.
Karyotypes.
1 Chapter 11 Complex Inheritance and Human Heredity 11.3 Chromosomes and Human Heredity.
11.3 CHROMOSOMES & HUMAN HEREDITY
Chromosomes and Karyotypes Chromosomes are comprised of a single, uninterrupted DNA molecule and proteins (histones) A karyotype is a visual display of.
Karyotypes. Karyotypes are pictures of homologous chromosomes lined up together during metaphase I of meiosis. There are 44 autosomes and 2 sex chromosomes.
Errors in Meiosis.  Non-disjunction is the failure of homologous chromosomes, or sister chromatids, to separate during meiosis. Nondisjunction may occur.
Chromosomes and Karyotypes
Meiosis Topics 4.2 and Assessment Statements 4.2.1State that meiosis is a reduction division of a diploid nucleus to form haploid nuclei Define.
Title: Chromosomal mutations 01 November 2015 Learning question: what can go wrong in meiosis and how can this be detected? Homework: STUDY!!!
Human chromosomes There are 46 chromosomes (23 homologous pairs) in each somatic cell 22 pairs of autosomes 1 pair of sex chromosomes XX = Female OR XY.
KARYOTYPING Honors Biology. What and How? Used as a way to “see” the chromosomes Pairs up homologous chromosomes Allows for detection of several genetic.
Abnormal Meiosis: Nondisjunction.
Chromosomes and Cell Reproduction Chromosome structure and role in development and reproduction.
Karyotyping Chromosomes are extracted from a cell, stained, photographed and paired for genetic analysis in the lab. Karyotypes are used to identify chromosomal.
Genetic Disorders Things Can Go Wrong With DNA and Chromosomes.
Prayer Next Prayer Attendance. Chapters
Cell Division (2) Meiosis: two-stage cell division in which the chromosome number of the parent cell is reduced by half. Meiosis is the process by which.
4.2.4 – Non-disjunction, karyotyping, chorionic villus sampling, amniocentesis, theoretical genetics Tyler and Tahjai.
Karyotyping Biology Miss Schwipperty. Questions  How many chromosomes come from your Father?  How many chromosomes come from your Mother?  What are.
Karyotypes and Nondisjunction
MEIOSIS AND CROSSING OVER Chromosomes are matched in homologous pairs Homologous chromosomes: the 2 members of a pair of chromosomes—contain genes for.
Meiosis IB Topics 4.2 and 10.2 Chapter 13 Campbell.
4.3 Alterations In Chromosome Structure and Number
MEIOSIS 3.3 & Meiosis: A reduction division of a diploid nucleus to form four haploid nuclei. This allows for a sexual life cycle in living organisms.
Gamete Formation & Genetic Variation. Gamete Formation The production of gametes is called __________________ and results in the formation of __________.
Sex Determination & Nondisjunction Disorders June 13, 2016.
Karyotypes copyright cmassengale.
Things Can Go Wrong With DNA and Chromosomes
Chromosomes and Karyotypes
Topic 4: Genetics 4.2 Meiosis  IB Biology SFP - Mark Polko.
Chromosomes Honors Biology.
Mutations & Their Implications
GT Biology March 8, 2011 Karyotypes.
Meiosis Topics 4.2 and 10.1.
Ch.7: Meiosis and Sexual Reproduction
3.3 Meiosis Alleles segregate during meiosis allowing new combinations to be formed by the fusion of gametes.
Chromosomes and Karyotypes
KARYOTYPES A diagram showing the arrangement of chromosomes aligned with their homologous chromosome Allows doctors to determine if an unborn child will.
Chromosomes and Karyotypes
Chromosomes and Karyotypes
Abnormal Meiosis.
MEIOSIS & Abnormal Meiosis
Sexual Reproduction Meiosis.
KARYOTYPES A diagram showing the arrangement of chromosomes aligned with their homologous chromosome Allows doctors to determine if an unborn child will.
Nondisjunction and Karyotypes
Notes: When Mistakes Occur
Presentation transcript:

Prokaryote vs. Eukaryote Chromosomes Prokaryotes have one chromosome consisting of a circular DNA molecule. Some prokaryotes also have plasmids but eukaryotes do not. Eukaryote chromosomes are linear DNA molecules associated with histone proteins. In a eukaryote species there are different chromosomes that carry different genes.

DNA and Chromosomes Eukaryote chromosomes are linear DNA molecules associated with histone proteins. Eukaryotic chromosomes contain DNA wrapped around proteins called histones. The strands of nucleosomes are tightly coiled and supercoiled to form chromosomes.

Structure of Nucleosomes Of eukaryote chromosomes The double helix has major and minor groves on its outer diameter. These groves expose chemical groups that can form hydrogen bonds. These chemical groups within DNA are bonded to by proteins. DNA is bonded to proteins called HISTONES. The diagram to the left is of a nucleosome: DNA is wound around and hydrogen bonded to eight histones. 146 DNA bases or 1.65 turns of the helix are associated with the 8 histones The combination of DNA and histones is secured by the 'H1 linker' protein.

Supercoiling of Eukaryote DNA Supercoiling condenses the DNA molecule by a factor of X 15,000 Histones are responsible for the packaging of DNA at the different levels (diagram left). The metaphase chromosome is an adaptation for mitosis and meiosis. . A little extra info:- The histones interact with the DNA structure to neutralize the acidity of this molecules. The DNA raps around the histones x 1.65 ( 146 base pairs)which means that although condensed in wrapping the DNA it is still accessible to polymerase molecules. This preserves the functionality of the DNA. This level of winding around the histones brings about a X 6.8 fold reduction in length. This is the so called 30nm fibre. However there is still a long way to go before achieving the 1600 (250 nm fibre) or the 10 000 reduction in the metaphase chromosome. Beads of histones still remain in regions being transcribed and also where there is polymerisation. It would appear that the histones of the nucleosome are just slightly displaces locally.

Prokaryote chromosomes Prokaryotes have one chromosome consisting of a circular DNA molecule. Some prokaryotes also have plasmids but eukaryotes do not.

Karyotypes

IB ASSESSMENT STATEMENT State that, in karyotyping, chromosomes are arranged in pairs according to their size and structure.

Gender Determination

Karyotyping is a standardized arrangement of all the chromosomes of a cell. Karyotypes are created by Medical Technicians using special biochemical techniques. In a karyotype, the chromosomes are arranged and displayed in a standard format where identical pairs are ordered by Size and position of centromere

Two things that can be deduced from Karyotypes Gender of the person Chromosomes abnormalities

IB Assessment Statement Explain that non-disjunction can lead to changes in chromosome number, illustrated by reference to Down syndrome (trisomy 21).

Chromosome disorder A disorder caused by an individual having more or less chromosomes than normal Chromosome abnormalities would occur during anaphase I and II of meiosis, when chromosomes failed to separate. This is called non-disjunction. In non-disjunction a gamete will have too many or too few chromosomes. If this gamete becomes fertilized the zygote will have a chromosome disorder.

Animation of Non-disjunction http://www.biostudio.com/d_%20Meiotic%20Nondisjunction%20Meiosis%20I.htm http://www.biostudio.com/d_%20Meiotic%20Nondisjunction%20Meiosis%20II.htm

3 chromosomes of chromosome 21 is down syndrome

Chromosome Abnormality Disorder Chromosome Abnormality Characteristics Down Syndrome (trisomy 21) 47 chromosomes 3 chromosomes of number 21 Age of mother influences the risk At maternal age 20 to 24, the risk is 1/1490; At age 40 the risk is 1/60, and at age 49 the risk is 1/11 poor muscle tone flat nasal bridge Most individuals with down syndrome have mental retardation The incidence of Down syndrome is estimated at 1 per 800 births an enlarged tongue Turner’s 45 chromosomes Normal female has XX. Turners syndrome only has one X. Short stature Low hairline Low-set ears Reproductive sterility The absence of a menstrual period 1 out of every 2500 female births

Klinefelter’s Syndrome 47 or more chromosomes A male w/ XXY or XXXY Affected males are almost always sterile, and some degree of language impairment may be present. possible characteristics vary widely and include little to no signs of affectedness, a lanky, youthful build and facial appearance, or a rounded body type with some degree 1 in 500 live male births Metafemale 47 Chromosomes XXX Triple X syndrome most often causes no unusual physical features or medical problems. Females with the condition are usually taller than average, and their weight may be low in comparison to their height 1/1000 female births

IB ASSESSMENT STATEMENT Analyse a human karyotype to determine gender and whether nondisjunction has occurred. Karyotyping can be done by using enlarged photographs of chromosomes.

IB Assessment Statement State that karyotyping is performed using cells collected by chorionic villus sampling or amniocentesis, for pre-natal diagnosis of chromosome abnormalities.

How is karyotypes done on unborn babies? Cells are obtained from unborn babies using two methods. Amniocentesis Chorionic villus sampling

Aminiocentesis A sample of fluid is removed from the amniotic sac around the fetus. To do this a hypodermic needle is inserted through the wall of the mother abdomen and the wall of the uterus. Amniotic fluid is removed, which contain fetus cells.

Once cells are obtained Chromosomes are visible in the metaphase stage of mitosis. A picture is taken of these chromosomes. The chromosomes are cut out and arrange into pairs according to their size and structure.

ttp://video.about.com/pregnancy/Amniocentesis.htm

Chorionic Villus Sampling Cells are removed from the fetal tissue in the placenta called chorionic villi. A hypodermic needle is inserted into the mother abdomen and uterus wall to obtain cells.

ttp://video.about.com/pregnancy/Chorionic-Villus-Sampling.htm

Once cells are obtained Chromosomes are visible in the metaphase stage of mitosis. A picture is taken of these chromosomes. The chromosomes are cut out and arrange into pairs according to their size and structure.