Characteristics showing delayed inheritance still conform with the principles of chromosomal genetics but are sidetracked by the ties of the parent
Delayed chromosomal inheritance
The ties are usually between the maternal parent and the offspring
Results from 2 important features of the egg but not the sperm:
The orientation of the mitotic spindle axis
The high cytoplasmic continuity between the egg and the oocyte with very little or no contribution from the sperm
Delayed chromosomal inheritance
Caspari's example of maternal influence in the flour moth Esphestia kuhnielle
Kynurenin
A diffusible, hormone-like substance involved in pigment synthesis
In some cases, maternal influence does not diminish during development but lasts throughout adult life
Inheritance of the direction of coiling of the snail Limnea peregra's shell
Dextral (right) or sinistral (left) coiling
Inheritance of the direction of coiling of the snail Limnea peregra's shell
F1 shows the same direction of coiling as the maternal parent
F2 are all dextrally coiled
F3 segregates 3 dextral: 1 sinistral
Dextral-sinistral alternative
Depends on a gene pair in which the allele for dextral is dominant
The developmental consequences of delayed gene action may also be detrimental, e.g. grandchildless mutation in Drosphila
Extrachromosomal inheritance
Cytoplasmic factors capable of self-perpetuation and independent transmission, considered genetic units fully equal to those in the chromosome
Extrachromosomal inheritance
Tends to be maternal because most of the zygote's cytoplasm is derived from the egg
Reciprocal crosses give different results, like delayed chromosomal inheritance
Unusual phenotypic ratios do not disappear after one generation
Plasmid inheritance
Perpetuation through DNA replication, a second system for the transmission of traits
Cytoplasmic inheritance in Chlamydomonas
Streptomycin resistance (sr) or sensitivity (ss) inherited in a regular Mendelian fashion
Cytoplasmic particles in Paramecium aurelia
Killer vs. sensitive trait determined by the gene K and the cytoplasmic particulate material called kappa
Chloroplasts
Responsible for photosynthesis
Structure, pigments, and enzyme systems can be affected by mutations
Capable of self-replication
Contain DNA, have their own genetic machinery
Mitochondria
Have their own DNA
Divide and reproduce by themselves
Explain the cytoplasmic continuity of neutral and suppressive petites in yeast
The human mitochondrial genome includes only 37 genes, 13 of which encode proteins important in cellular respiration
Genetic disorders associated with mitochondrial DNA in humans
Progressive external opthalmoplegia
Kearn-Sayre Syndrome
Pearson Syndrome
Leber Hereditary/Optic Neuropathy
Cytoplasmic-nuclear male sterility
Male sterility due to cytoplasmic factors (e.g. genes in the mitochondrial genome) that can interact with nuclear genes (e.g. fertility restorer genes) to restore male fertility
Cytoplasmic-nuclear male sterility is widely used in the production of F1 hybrid seeds of many crop species
Cytoplasmic - Nuclear Male Sterility
Male sterility due to cytoplasmic factors that can interact with nuclear genes to restore fertility
Cytoplasmic male sterility (CMS) has been observed in many plant species
Male sterility is due to some cytoplasmic factors (e.g., genes in the mitochondrial genome)
These mitochondrial genes can interact with genes in the nuclear genome (e.g., fertility restorer genes) and restore male fertility despite sterile cytoplasm
This phenomenon is widely used in the production of F1 hybrid seeds of many crop species, e.g., rice, corn, etc.
The F1 hybrids are more vigorous and productive than the pure lines or open pollinated varieties because of hybrid vigor or heterosis
Dominance hypothesis
There is accumulation of favorable parental dominant genes in the hybrid
Overdominance hypothesis
Heterozygotes are more vigorous, productive, and perform well over a range of environments than either homozygotes
Without CMS, hybrid seed production requires emasculation/disabling of pollen before anther dehiscence and stigma receptivity
Using CMS lines as the female parent restorer line (R line) as the male parent, the tedious process of emasculation/ detasseling is bypassed in the F1 hybrid seed production
Plasmids of extracellular origin
They are not normal or indispensable components of the normal cell
They can be transmitted from infected to uninfected individuals by cell extracts from the former
They are not capable of moving in and out of the chromosomal DNA of the host and can exist in the nucleus of the cytoplasm of the host
Infective heredity
Heritable traits transmitted through virus-like particles
Infective heredity
Mammary cancer susceptibility in mice
CO2-sensitivity in Drosophila
Episomes
Genetic elements that may exist either as an integral part of a chromosomal DNA molecule of the host or as an independently replicating DNA molecule (plasmid), free of the host chromosome
The pattern of transmission for a phenotype based on any of the various potential extranuclear systems cannot be predicted with certainty
The most feasible procedure is to examine whether there are instances where transmission is such that the chromosomal basis is either ruled out or at least unlikely
Criteria for extrachromosomal inheritance
Difference in reciprocal cross results
Maternal inheritance
Non-mappability
Non-Mendelian segregation
Indifference to nuclear substitution
When one follows the transmission of characteristics based on chromosomal heredity, the reciprocal crosses are ordinarily identical, except in cases of sex-linked genes
Maternal inheritance
A characteristic form of difference in the results of reciprocal crosses where the progenies show the characteristics of their female parent
If the chromosomal differences can be ruled out, maternal inheritance usually implies transmission through the cytoplasm