5 Human Chromosomes and Chromosome Behavior. 2 Human Chromosomes Humans contain 46 chromosomes, including 22 pairs of homologous autosomes and two sex.

5Human Chromosomes

and Chromosome Behavior

2

Human Chromosomes• Humans contain 46 chromosomes, including 22

pairs of homologous autosomes and two sex chromosomes

• Karyotype = stained and photographed preparation of metaphase chromosomes arranged according to their size and position of centromeres

3Fig. 5.3 1-10

4Fig. 5.3 11-y

5

Human Chromosomes• Each chromosome in karyotype is divided into

two regions (arms) separated by the centromere

• p = short arm (petit); q = long arm

• p and q arms are divided into numbered bands and interband regions based on pattern of staining

• Within each arm the regions are numbered.

6

Centromeres• Chromosomes are classified according to the relative

position of their centromeres• In metacentric it is located in middle of chromosome• In submetacentric—closer to one end of chromosome• In acrocentric—near one end of chromosome• Chromosomes with no centromere, or with two

centromeres, are genetically unstable

7Fig. 5.3

8

Human X Chromosome• Females have two copies of X chromosome• One copy of X is randomly inactivated in all

somatic cells• Females are genetic mosaics for genes on the X

chromosome; only one X allele is active in each cell

• Barr body = inactive X chromosome in the nucleus of interphase cells

• Dosage Compensation = dosage equalization for active genes

9Fig. 5.7

10

Human Y Chromosome• Y chromosome is largely heterochromatic• Heterochromatin is condensed inactive chromatin• Important regions of Y chromosome:

pseudoautosomal region = region of shared X-Y homology

SRY=master sex controller gene which encodes testis determining factor (TDF) for male development

The pseudoautosomal region of the X and Y chromosomes has gotten progressively shorter in evolutionary time.

11Fig. 5.10

12

Human Y Chromosome• Y chromosome does not undergo recombination

along most of its length, genetic markers in the Y are completely linked and remain together as the chromosome is transmitted from generation to generation

• The set of alleles at two or more loci present in a particular chromosome is called a haplotype

• The history of human populations can be traced through studies of the Y chromosome

13

Abnormal Chromosome Number• Euploid = balanced chromosome abnormality = the

same relative gene dosage as in diploids (example: trisomics)

• Aneuploid = unbalanced set of chromosomes = relative gene dosage is upset (example: trisomy of chromosome 21)

• Monosomic = loss of a single chromosome copy Polysomic = extra copies of single chromosomes

• Chromosome abnormalities are frequent in spontaneous abortions.

14

Abnormal Chromosome Number• Monosomy or trisomy of most human autosomes

unviable. There are three exceptions: trisomies of 13, 18 and 21

• Down Syndrome is a genetic disorder due to trisomy 21, the most common autosomal aneuploidy in humans

• Frequency of Down Syndrome increases with mother’s age

• Amniocentesis = fetal cells are analyzed for abnormalities of chromosome number and structure

• Chorionic villus sampling (CVS) = cells from a zygote-derived embryonic membrane (the chorion) analyzed

15

Abnormal Chromosome Number

• Trisomic chromosomes undergo abnormal segregation

• Trivalent = abnormal pairing of trisomic chromosomes in cell division

• Univalent = extra chromosome in trisomy is unpaired in cell division

16Fig. 5.13

17

Sex Chromosome Aneuploidies• An extra X or Y chromosome usually has a relatively

mild effect

• Trisomy-X = 47, XXX (female)

• Double-Y = 47, XYY (male)

• Klinefelter Syndrome = 47, XXY (male, sterile)

• Turner Syndrome = 45, X (female, sterile)

18

Chromosome Deletions• Deletions = missing chromosome segment

• Polytene chromosomes of Drosophila can be used to map physically the locations of deletions

• Any recessive allele that is uncovered by a deletion must be located inside the boundaries of the deletion = deletion mapping

• Large deletions are often lethal

19Fig. 5.16

20

Gene Duplications• Duplication = chromosome segment present in multiple copies• Tandem duplications = repeated segments are adjacent • Tandem duplications often result from unequal crossing-over

due to mispairing of homologous chromosomes during meiotic recombination

Fig. 5.17

21

Red-Green Color Vision Genes• Genes for red and green pigments are close on X-

chromosome

• Green-pigment genes may be present in multiple copies on the chromosome due to mispairing and unequal crossing-over

• Unequal crossing-over between these genes during meiotic recombination can also result in gene deletion and color-blindness

• Crossing-over between red- and green-pigment genes results in chimeric (composite) gene

22

Chromosome Inversions• Inversions = genetic

rearrangements in which the order of genes in a chromosome segment is reversed

• Inversions do not alter the genetic content but change the linear sequence of genetic information

• In an inversion heterozygote, chromosomes twist into a loop in the region in which the gene order is inverted Fig. 5.22

23

Chromosome Inversions

• Paracentric inversion = does not include centromere;

• Crossing-over within a paracentric inversion loop during recombination produces one acentric (no centromere) and one dicentric (two centromeres) chromosome

24Fig. 5.23

25

Chromosome Inversions • Pericentric inversion = includes centromere• Crossing-over within a pericentric inversion loop during

homologous recombination results in duplications and deletions of genetic information

26

Reciprocal Translocations• A chromosomal aberration resulting from the

interchange of parts between nonhomologous chromosomes is called a translocation

• There is no loss of genetic information but the functions of specific genes may be altered

• Translocations may produce position effects = changes in gene function due to repositioning of gene

• Gene expression may be elevated or decreased in translocated gene

27

Reciprocal Translocation• Heterozygous translocation = one pair interchanged,

one pair normal

• Homozygous translocation = both pairs interchanged

Fig. 5.25

28

Reciprocal Translocations• Synapsis involving heterozygous reciprocal

translocation results in pairing of four pairs of sister chromatids = quadrivalent

• Chromosome pairs may segregate in several ways during meiosis, with three genetic outcomes:

• Adjacent-1 segregation: homologous centromeres separate at anaphase I; gametes contain duplications and deletions

29

Reciprocal Translocation

• Adjacent-2 segregation: homologous centromeres stay together at anaphase I; gametes have a segment duplication and deletion

• Alternate segregation: half the gametes receive both parts of the reciprocal translocation and the other half receive both normal chromosomes; all gametes are euploid, i.e have normal genetic content, but half are translocation carriers

30

Reciprocal Translocation• The duplication and deficiency of gametes produced

by adjacent-1 and adjacent-2 segregation results in the semisterility of genotypes that are heterozygous for a reciprocal translocation

• The frequencies of each outcome is influenced by the position of the translocation breakpoints, by the number and distribution of chiasmata, and by whether the quadrivalent tends to open out into a ring-shaped structure on the metaphase plate

31Fig. 5.26

32

Robertsonian Translocation

• A special case of nonreciprocal translocation is aRobertsonian translocation = fusion of two acrocentric chromosomes in the centromere region

• Translocation results in apparent loss of one chromosome in karyotype analysis

• Genetic information is lost inthe tips of the translocatedacrocentric chromosomes

Fig. 5.27

33

Robertsonian TranslocationRobertsonian translocations are an important risk factor to be considered in Down syndrome. When chromosome 21 is one of the acrocentrics in a Robertsonian translocation, the rearrangement leads to a familial type of Down syndrome

The heterozygous carrier is phenotypically normal, but a high risk of Down syndrome results from aberrant segregation in meiosis

Approximately 3 percent of children with Down syndrome are found to have one parent with such a translocation

34

Polyploidy• Polyploid species have multiple

complete sets of chromosomes

• The basic chromosome set, from which all the other genomes are formed, is called the monoploid set

• The haploid chromosome set is the set of chromosomes present in a gamete, irrespective of the chromosome number in the species.

Fig. 529

35

Polyploidy• Polyploids can arise from genome duplications

occurring before or after fertilization

• Two mechanisms of asexual polyploidization: the increase in chromosome number takes place in meiosis

through the formation of unreduced gametes that have double the normal complement of chromosomes

the doubling of the chromosome number takes place in mitosis. Chromosome doubling through an abortive mitotic division is called endoreduplication

36

Polyploidy• Autopolyploids have all chromosomes in the

polyploid species derive from a single diploid ancestral

• Allopolyploids have complete sets of chromosomes from two or more different ancestral species

• Chromosome painting = chromosomes hybridized with fluorescent dye to show their origins

• Plant cells with a single set of chromosomes can be cultured

37Fig. 5.31

38

Polyploidy• The grass family illustrates the importance of

polyploidy and chromo-some rearrangements in genome evolution

• The cereal grasses (rice, wheat, maize, millet, sugar cane, sorghum, and other cereals) are our most important crop plants

• Their genomes vary enormously in size: from 400 Mb found in rice to 16,000 Mb found in wheat

39

Polyploidy• In spite of the large variation in chromosome

number and genome size, there are a number of genetic and physical linkages between single-copy genes that are remarkably conserved in all grasses amid a background of rapidly evolving repetitive DNA

• Each of the conserved regions (synteny groups) can be identified in all the grasses and referred to a similar region in the rice genome.