In Madeleine L'Engle's children's novel A Wrinkle in Time, the mitochondria in one of the characters starts to die. Describe what would happen to people who lost their mitochondria, and explain why it would happen.© BrainMass Inc. brainmass.com October 24, 2018, 9:42 pm ad1c9bdddf
Mitochondria is a powerhouse of cell. It is a center of Krebs cycle or respiration in which energy in the form of ATP is formed. Each mitochondrion is covered by a double membrane envelope. Outer membrane is permeable to many metabolites due to presence of porins. Inner membrane is selectively permeable. Cristae are formed by infoldings of inner membrane. ...
This solution discusses mitochondria as the power house of the cell and the consequences of dying mitochondria on the bodies energy sources in 223 words.
I am looking for help answering the following multiple choice questions regarding following a trait over generations of a family.
Please help me answer the following questions about a mutation in mitochondrial DNA and how that mutation can affect the phenotype. The questions need me to draw a pedigree following this trait throughout generations and then use the information to answer multiple choice questions
The following information pertains to questions 13-15
In 19995, Tiranti et al. (human Molecular Genetics 4:1421-1427) reported an instance of mitochondrial inheritance for hearing loss in a human pedigree. All siblings in a family of four (one male and three females) had hearing loss. The parents were deceased, so the parental phenotypes were unknown, although the parents were known to be first cousins. All four siblings were married to unrelated spouses, none of whom had hearing loss. The oldest sibling was female and had four children, all females and none with hearing loss. The second oldest was also female and had three children, two males and a female. Only the female child had hearing loss. The third sibling was male and had three children, two males and a female and none with hearing loss. The fourth sibling was female and had four children, three males and a female, all with hearing loss. (hint: to help yourself with your analysis, draw a pedigree of this family).
The researchers discovered a mutation in the DNA in one of the two mitochondrial serine tRNA genes. Below is a portion of the normal and mutant sequences of the tRNA gene:
Tirani et al. measured the proportion of mutant mitochondrial DNA in the somatic cells of members of this family with and without hearing loss. They found that the proportion of the mutant mitochondrial DNA in those individuals who had hearing loss ranged from 66 percent to 100 percent. Among those who did not have hearing loss, the proportion of mutant mitochondrial DNA ranged from 0 percent to 70 percent.
13) Only one of the siblings (a female) had 100 percent mutant mitochondrial DNA. Based on the information above, which of the siblings had 100 percent mutant mitochondrial DNA?
a) the first (oldest) sibling
b) the second sibling
c) one third sibling
d) the fourth (youngest) sibling
14) Mutations in mitochondrial DNA are usually transmitted in a uniparental-maternal fashion in mammals. Why then do some of the remote siblings with hearing loss have children who do not have hearing loss?
a) The females who had offspring without hearing loss were heteroplasmic.
b) There are two mitochondrial serine tRNA genes. The other tRNA gene sometimes compensates for the loss of function in the mutant tRNA gene.
c) Biparental inheritance of mitochondrial DNA caused some of the offspring to escape hearing loss.
d) None of the above
15) Which of the following is the most probable cause of this mutation?
a) slippage during DNA replication
b) tautomeric shift
d) SOS mutagenesis