ch 5 nonmendelian inheritance Flashcards
maternal effect
an inheritance pattern for certain nuclear genes in which the gene type of the mother directly determines the phenotypic traits of her offspring
reciprocal cross
a pair of crosses in which the traits of the two parents differ with regard to sex; for example, one cross could be a red-eyed female fly and a white-eyed male. and the the reciprocal cross would be a red-eyed male fly and white-eyed female fly
epigenetics
the study of mechanisms that lead to changes in gene expression that can be passed from cell to cell and are reversible but do not involve a change in the dna sequence
dosage compensation
the phenomenon observed in species with sex chromosomes, in which one of the sex chromosomes is altered so that males and females have similar levels of gene expression, even though they do not have the same complement of sex chromosomes
x-chromosome inactivation (XCI)
a process in which mammals equalize the expression of x-linked genes by randomly turning off one x chromosome in the somatic cells of females
barr body
a structure in the interphase nuclei of somatic cells of female mammals that is a highly condensed x-chromosome
lyon hypothesis
a hypothesis to explain the pattern of x-chromosome inactivation seen in mammals; initially, both x-chromosomes are inactive; however, at an early stage of embryonic development, one of the two x chromosomes is randomly inactivated in each somatic cell
clone
- a group of genetically identical cells that were derived from a single cell
- an individual that has been produced from a somatic cell of another individual, such as the sheep dolly
- many copies of dna fragment that are propagated within a vector or produced by pcr
x-inactivation center (Xic)
a site on the x chromosome that appears to play a critical role in X-chromosome inactivation
genomic imprinting
a pattern of inheritance that involves a change in a single gene or chromosome during gamete formation; depending on whether the modification occurs during spermatogenesis or oogenesis, imprinting governs whether an offspring will express a gene that has been inherited from its mother or father
monoallelic expression
in the case of genomic imprinting. refers to the phenomenon that only one of the two alleles of a given gene is transcriptionally expressed
dna methylation
a regulatory mechanism in which an enzyme covalently attaches a methyl group (–CH3) to a base in dna; in eukaryotes. the base is cytosine; in prokaryotes. both adenine and cytosine can be methylated
imprinting control region (ICR)
a dna region that is differentially methylated and plays a role in genomic imprinting
nuclear genes
genes that are located on chromosomes found in the cell nucleus of eukaryotic cells
extranuclear inheritance
(also called cytoplasmic inheritance) the inheritance of genetic material that is not found within the cell nucleus