Answer:
In compare to eukaryotes,prokaryotes are morphologically simpler,more evolutionary primitive,less sensitive to physical environment.
Explanation:
Prokaryotes are unicellular organism which don't possess cell organelle like nucleus,mitochondria,Endoplasmic reticulum,golgi body, etc.
They are the first living organism in the primitive earth and the genetic components are located in the cytoplasm which is enclosed by cell membrane.
prokaryotes contain 3 domains that are Archaea, bacteria and eukarya.
The cytoplasm is enclosed by cell membrane.
Molecular studies have reveal that eukaryotes are evolved from prokaryotes.
Some prokaryotes bear long projection which helps them for locomotion,called as flagellum.This is present in gram positive and gram negative bacteria.
The mutation as the Hardy- Weinberg equation assumes that there would be no evolutionary pressures such as mutations. Hardy- Weinberg represents an 'ideal' where the allele frequencies would remain constant
The rodents mutate the new grey allele.
Answer:
Genetic mapping for unequivocal identification of the potentially causative mutation
Explanation:
Galactosemia is a genetic disorder caused by mutations in the Galactose-1-phosphate uridylyltransferase (GALT) gene, which encodes an enzyme involved in the metabolism of galactose. Gene mapping is a technique widely used in genetics to identify the position of one locus a chromosome by using molecular markers to estimate genetic distances. Genetic mapping provides useful evidence in order to identify when a disease that is transmitted from parent to offspring can be associated with one or more genes and then determine which gene/s is/are responsible for this condition.
The right answer is C.
A genetic disease is called autosomal dominant transmission when
:
* The morbid allele ("sick" version, mutated of the gene in question) is on a non-sexual chromosome (neither X nor Y).
* The presence of a single morbid allele is sufficient for the disease to express itself.
The morbid allele is transmitted by either the father or the mother (or both, if they have the same inherited autosomal dominant genetic disease). Anyone with one of their affected parents is affected.
Jackson-Weiss syndrome is indeed an autosomal dominant disease characterized by a malformation of the feet, craniosynostosis of varying degrees, facial abnormalities, enlargement of the big toes and normal hands.
