DNA in a Cell and how is it arranged! Mike Clark, M.D.

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Presentation transcript:

DNA in a Cell and how is it arranged! Mike Clark, M.D.

Amount of Genetic Material in a Cell Before we discuss mitosis or meiosis – let’s examine how much genetic material is in a cell. There are two divisions of cells in the human body- somatic cells and gametes (sex cells) Somatic cells have twice the amount of genetic material of the gametes

Somatic Cells Somatic cells are all the human body cells except the gametes Somatic cells have 46 pieces of genetic material (46 DNA pieces) – organized into 23 pairs 23 pieces (one set) of the genetic material was given to your cells by your mother and the other 23 pieces (the other set) was given to you by your father

How do we identify a set of Genetic Material Most authors say that we have 46 chromosomes – which is true – but if you notice I use the term genetic material rather than chromosome because remember that a chromosome is a certain folding pattern of the DNA – thus not always is the DNA folded into the chromosome fold – as a matter of fact most of the time it is not folded into the chromosome fold.

DNA Folding in a Cell The average human cell nucleus has a diameter of approximately 5 micrometers (5 x meter or 5 millionths of a meter) If we stretch out the DNA in a somatic cell in the human – it is approximately 2 meters in length – so you can see we need a heck of a good folding system for the DNA. The DNA must be folded good so it can be read properly.

Figure 3.30 Metaphase chromosome (at midpoint of cell division) Nucleosome (10-nm diameter; eight histone proteins wrapped by two winds of the DNA double helix) Linker DNA Histones (a) (b) 1 DNA double helix (2-nm diameter) 2 Chromatin (“beads on a string”) structure with nucleosomes 3 Tight helical fiber (30-nm diameter) 5 Chromatid (700-nm diameter) 4 Looped domain structure (300-nm diameter)

Examination of Genetic Material The chromosome is thick enough to be seen using the light microscope The genetic material (DNA) is folded into the chromosome fold during the M-phase (mitosis or meiosis) of the cell divisional cycle. The genetic material folds from the loop domain fold (too thin to be seen under light microscope) to the chromosome fold during the phases of prophase and metaphase – which are subdivisions of the cell’s M-phase These prophase and metaphase stages will be discussed in the lecture on mitosis

How are the different chromosomes distinguished? Human chromosomes must be determined one from another because each chromosome carries a different set of vital genes – lose a chromosome and lose those genes – thus lose the ability to make those necessary proteins Scientist have assigned the various chromosomes certain numbers Chromosomes are numbered 1 – 23 The 23 rd chromosomes are the sex chromosomes (X versus Y) – the first 22 chromosomes are termed “autosomes”

Sets of Chromosomes in Human Cells A karyotype is an ordered display of the pairs of chromosomes from a cell The two chromosomes in each pair are called homologous chromosomes, or homologs – non- identical are termed “heterologous pairs” Chromosomes in a homologous pair are the same length and carry genes controlling the same inherited characters A different chromosomes are identified and classified in accordance with their individual (1) lengths (2) centromere positions and (3) unique staining patterns

Fig. 13-3b TECHNIQUE Pair of homologous replicated chromosomes Centromere Sister chromatids Metaphase chromosome 5 µm

Ploidy Ploidy refers to a full set of chromosomes – a full set can also be represented by the letter n Thus one ploidy would relate to one complete set of chromosomes (23) with one representative chromosome from each of the 23 different types – a representative from chromosome one, a representative from chromosome two – as so on till a representative from all 23. A somatic cell is diploid (2n) with two full sets of genetic material (one set from dad and one from mom) A gamete has ½ the amount of genetic material as a somatic cell – it is termed haploid (1n)

Karyotype A karyotype is an ordered display of the pairs of chromosomes from a cell The two chromosomes in each pair are called homologous chromosomes, or homologs

Fig APPLICATION TECHNIQUE Pair of homologous replicated chromosomes 5 µm Centromere Sister chromatids Metaphase chromosome A Karyotype pictorially displaying all of the chromosomes in a somatic cell.

Fig. 13-3b TECHNIQUE Pair of homologous replicated chromosomes Centromere Sister chromatids Metaphase chromosome 5 µm

Discussion of a Chromosome/Chromatid There are two forms of a chromosome The singlet non-attached type chromosome The doublet (attached) type –the chromosome/chromatid form Both forms are termed a chromosome

The doublet type – a chromosome/chromatid During the S-phase in the cell divisional cycle – DNA is duplicated (as previously discussed) Immediately after the S-phase (Synthesis phase) in the cell divisional cycle – there is twice as much DNA – each chromosome is duplicated The new duplicate and the original stay temporarily attached to one another–thus two pieces of DNA remain temporarily attached Each attached piece of DNA is termed a “chromatid” more especially “sister chromatids” The two attached chromatids are termed one chromosome

Adenine Thymine Cytosine Guanine Old (template) strand Two new strands (leading and lagging) synthesized in opposite directions DNA polymerase Lagging strand Leading strand Free nucleotides Old strand acts as a template for synthesis of new strand Chromosome Helicase unwinds the double helix and exposes the bases Old DNA Replication fork DNA replication is a semi-conservative process. When DNA replicates the two half ladder strands of DNA separate into two strands and the enzyme DNA polymerase assists to build a new complimentary half DNA to the original strand of DNA. Thus when DNA is synthesized – there really is no completely new chromosome because each chromosome is made-up of half of the old chromosome.

Fig µmChromosomes Chromosome duplication (including DNA synthesis) Chromo- some arm Centromere Sister chromatids DNA molecules Separation of sister chromatids Centromere Sister chromatids Duplicated DNA is attached- each is termed a chromatid

Each attached piece of DNA is termed a “chromatid” more especially “ a sister chromatid” – this is the doublet form of DNA The two attached chromatids are termed one chromosome When the two doublets break apart (separate) each of the now split doublets are termed a chromosome – but a singlet version Thus the term chromatid/chromosome and the term chromosome are a matter of semantics

Fig µmChromosomes DNA molecules Separation of sister chromatids by the breaking of the centromere. Duplicates are now separated each separate piece is also termed a chromosome. Centromere holding chromatids Together.