1. Types of Chromosome Mutations

2. Chromatin and Gene Expression
Heterochromatin
Contains methylated histones (H3)
Associated with heterochromatin protein-1 (HP-1)
Transcriptionally Active Euchromatin
Contains hyperacetylated histones
Prevention of Heterochromatin Formation
DNA elements (barrier insulators) promote binding of histone acteyltransferase

3. Gene Silencing is Caused by the Spread of Heterochromatin
When a chromosome mutation places a gene next to heterochromatin, the gene can become inactivated.
Inversion, deletion, duplication, and translocation can place a gene next to heterochromatin.

4. Heterochromatin May Spread Farther in Some Cells Than in Others

5. Position-effect Variegation
A heterozygote for a gene and a translocation can show variegated phenotype for that gene.
Position-effect variegation is exhibited by this w+/w heterozygote.
Wild-type allele is no longer wild-type in its expression in some of the eye facets.
Any chromosomal change that places a locus next to heterochromatin can result in inactivation of that gene.
A tissue or organ that is comprised of a mixture of cells that express one or the other phenotype exhibit this variegation.

6. Types of Chromosome Mutations

7. The fates of a million implanted human zygotes
50% of spontaneous abortions are associated with chromosome abnormalities.
Over half of these are trisomics, with trisomy 21 accounting for 9% of them.
18% of abnormalities are the Turner condition.
~ 0.6% of birthed infants have chromosome abnormalities.
~ 36% of birthed infants with chromosome abnormalities are aneuploidy of sex chromosome.
~ 23% of birthed infants with chromosome abnormalities are trisomics.

8. Relationship between Genotype and Phenotype
Molecular Basis for
Relationship between Genotype and Phenotype
genotype
DNA
DNA sequence
transcription
RNA
translation
amino acid
sequence
protein
function
phenotype
organism