Answer:
<em>Hox </em>Gene
Explanation:
First, you're question is very vital, there are many ways in classifying along with identifying all living organisms that includes; morphological analysis, molecular systematics (studying the similarities and differences of the genetic data such in the sequences of DNA, RNA, and rRNA ), homology, cladistics, etc. based on phylogenetic tree, which the study of the evolutionary among various species.
But through it said that all living organisms shared one common ancestor. However, what makes them different from one to another is the homeotic genes that called <em>Hox </em>Genes; which specify the fate of a particular segment or region of the body, meaning the number and arrangements of the<em> Hox</em> genes varies considerably among different types of animals.
For instance, Sponges have at least one homologous to<em> Hox</em> genes, also insects have nine or more <em>Hox </em>genes resulting in multiple <em>Hox </em>genes occur in a cluster in which the genes are close to each other along a chromosome. Therefore, increases in the number of<em> Hox</em> genes have been instrumental in the evolution of many animals species with greater complexity in body structure.
Overall, more <em>Hox</em> genes, more complexity in body structure resulting in the differences of their morphological structure.
Hope that answered your question!
Spongy bone has trabecular which serve as reinforcing plates against a force. The loss of spongy bones causes weakening of the internal support that the compact bone requires and the entire bone breaks.
Answer: False
Explanation:
The urethra is a tube which runs from the bladder to the end of the penis. It functions by carrying the urine and semen outside the male body.
Urethra is made of two components. Prostatic urethera is the part that runs from the bladder through the prostrate.
The penis is only organ which carries both the fluids out of the body.
Answer:
Hemophilia is a x-linked recessive inherited bleeding disorder. in this disease blood does not clot properly due to the decreased level of blood clotting factor VIII (8) or factor IX (9).
In x-linked recessive condition, the disease is transmitted from father (affected male) to his daughter and mother (affected female) to her son and skip of generation getting affected is also occurs.
- there will be 50% chance of her (S.R.) each son to be affected with hemophilia.
Explanation:
Hemophilia is caused due to mutation of one gene which is responsible for the making of proteins of blood coagulation factor viii or ix. the affected person bleeds continuously from any injury and that can cause serious issues.
here,
grandfather of s.r is affected (xₐy) and grandmother is normal (xx) will produce
↓
s.r's mother who is a carrier (xₐx) [as xₐy and xx will produce 100% carrier xₐx daughter]
↓
s.r's mother is a carrier (xₐx) but her father is normal (xy) will produce,
↓
s.r who has 50% chance of being carrier (xₐx) and 50% chance of being normal (xx) [as she is the only child] and she has a normal (xy) partner, they will give,
↓
- if s.r is a carrier (xₐx) then one of her son will be affected (xₐy) [as xₐx and xy =xₐy]
- if s.r is normal (xx) then her son will be normal (xy) [as xx and xy will give xy]
here,<u> 50% chance of her son to be affected with hemophilia</u> [as S.R of being affected is more considerable].
