According to the lac operon model proposed by jacob and monod, what is predicted to occur if the operator is removed from the operon?

only lacy would be transcribed.
the lac operon would be transcribed constitutively.
galactosidase permease would be produced, but would be incapable of transporting lactose.
only lacz would be transcribed.

The right answer is The lac operon would be transcribed constitutively.

An operator is a nucleic acid segment to which a regulatory protein that modulates downstream gene expression is bound. it can either stimulate or inhibit the production of the gene product thus controlled.

If the operator is absent, there will be no more regulation of the operon, so the transcription of the operon will not be regulated, and the synthesis will be continuous and constitutive.

condensation. good luck!

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.