Segments of DNA transferred from parent go offspring are called

At very large distances from the Sun, its corona turns into the solar wind.<br> True<br> False

Illusion [34]

Answer:

the question really didnt make sense to me so false..

Explanation:

false

5 0

2 years ago

How many active volcanoes in Luzon , Visayas and Mindanao?

katrin [286]

There are currently
22 active volcanoes in Luzon
428 in Visayas
and 20 in mindanao

8 0

2 years ago

Classify the following characteristics depending on if they describe events occurring in mitosis, meiosis I, or meiosis II.

Temka [501]

Answer:

Mitosis events are:

Results in 2 genetically identical

diploid nuclei

A diploid number of sister

chromatids align at the spindle

equator during metaphase

Meiosis I events are:

Results in 2 genetically diverse

haploid nuclei

Homologous chromosomes align

at the spindle equator during

metaphase

Homologous chromosomes pair

up during prophase

Crossing-over occurs during

synapsis

Meiosis II events are:

Results in 4 genetically diverse

haploid nuclei

A haploid number of homologous

chromosomes align at the spindle

equator during metaphase

Explanation:

Mitosis is a type of cell division which produces two daughter cells that are genetically identical to the parent cell. In mitosis, the chromosome number of the parent cell is maintained in the daughter cells i.e. a diploid cell (2n) will undergo mitosis to produce two diploid (2n) daughter cells. During mitotic division, sister chromatids (replicated chromosomes) are involved in the division stages. i.e. diploid sister chromatids align at the equator of the cell during Metaphase and also sister chromatids are separated or pulled apart to opposite poles during Anaphase.

Meiosis, on the other hand, is a kind of cell division that results in daughter cells with a reduced number of chromosome (by half). Since the chromosome number is reduced, meiosis occurs in a two step division process viz: Meiosis I and II.

Meiosis I produces two genetically different daughter cells. The daughter cells have a reduced number of chromosomes i.e. from diploid (2n) to haploid (n). Meiosis I involves homologous chromosomes (similar but non-identical chromosomes received from each parent) which pair up to form a TETRAD structure in the Prophase stage. This structure allows for an exchange of chromosomal segment between non-sister chromatids of homologous chromosomes, a process called CROSSING-OVER. Crossing-over is what makes the daughter cells genetically different from the parent cell. Homologous chromosomes also aligns at the equator of the cell during Metaphase and later separates during Anaphase.

Meiosis II divides the two daughter cells produced in meiosis I into four genetically different daughter cells. Since the chromosome number has been reduced from diploid (2n) to haploid (n) in meiosis I when homologous chromosomes separate, haploid sister chromatids are involved in the stages of meiosis II i.e. haploid sister chromatids align at the equator of the cell during Metaphase and eventually becomes pulled apart during Anaphase.

5 0

2 years ago

WILL MARK BRAINLIEST AND GIVE 25 POINTS Explain how you linked the predator and its prey to a specific environment.

qwelly [4]

Answer:

The mouse and shrew bones were common to all three owls so they were not useful in identifying environments. The gopher bones were unique to the great grey owl of Alaska. Gophers are rodents that are successful in areas with soft soil and lots of grass, so the gopher and this owl would be found in the meadows and evergreen forests of Alaska. The bat was unique to the barking owl of Australia. The bat would be found in woodland habitats where there are many trees the bat can hang from. The gull bones were unique to the short-eared owl of Cuba. Gulls are wetland birds, so the gull and this owl would be found in marshes and coastal areas.

7 0

2 years ago

A polypeptide in a wild type microbe contains the sequence Leu-Pro-Tyr-Ser-Pro. A phenotypic variant of the species has the pept

Katen [24]

Answer:

The mentioned case is an illustration of the missense mutation. A missense mutation is a kind of nonsynonymous substitution, that is, it is a mutation in which a variation in a solitary nucleotide leads to the formation of a codon, which encrypts for a distinct kind of amino acid.

When a missense mutation takes place within a DNA, a modification in one of the RNA codon sequences results at the time of transcription. This change in codon will ultimately result in the formation of a different amino acid, which gets presented within a protein at the time of translation. Like in the given case, a change in codon resulted in the substitution of the amino acid tyrosine with an amino acid cysteine.

8 0

3 years ago