Principles of inheritance and variation Flashcards

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1
Q

Gene

A

it is the basic unit of inheritance. contains the information on a particular trait

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2
Q

allelles

A

allelles are genes with 2 contrasting characteristics

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3
Q

homozygous

A

both allelles are identical

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4
Q

heterozygous

A

both allelles are non identical

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5
Q

dominant allelle

A

it is the allelle that expresses itself in homozygous as well as heterozygous.

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6
Q

recessive allelle

A

The factor which fails to express itself in the presence of its contrasting allele. A recessive factor expresses itself only in homozygous condition

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7
Q

Hybrid:-
Monohybrid cross:-
Dihybrid cross:-

A

The offspring produced by a cross between two individuals differing in one or more characters. Eg. Tt
Cross between two parents differing in one pair of contrasting characters. Eg. Tall * Dwarf
Cross between two parents differing in two pairs of contrasting characters. Eg. Tall Red * Dwarf White

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8
Q

true breeding line

A

having undergone continuous self pollination
ii. shows stable trait inheritance and expression for several
generations

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9
Q

LAW OF DOMINANCE

A

Characters are controlled by discrete units called factors.
Factors occur in pairs.
In a dissimilar pair of factors,one member of the pair dominates (dominant) the other (recessive)

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10
Q

LAW OF SEGREGATION

A

Two alleles of a pair representing a character, will segregate or separate from each other during gamete formation , so that a gamete receives only one of the two factors (never both).
The paired condition is restored during gamete fusion.

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11
Q

Mendel’s Law of Independent Assortment

A

When two pairs of traits are combined in a hybrid, segregation of one pair of characters is independent of other pair of characters”.

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12
Q

INCOMPLETE DOMINANCE

A

Type of inheritance in which one allele is not completely dominant over the other.

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13
Q

MULTIPLE ALLELISM

A

Presence of more than two alleles for a gene

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14
Q

PLEIOTROPY

A

Phenomenon in which single gene exhibits multiple phenotypic expression.
Such a gene is called a pleiotropic gene.

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15
Q

Morgan worked with the tiny fruit flies Drosophila melanogaster.

A

. They could be grown in simple synthetic medium in the lab.
2. They complete their life cycle in about two weeks.
3. Single mating produces large number of progeny flies.
4. There is clear differentiation between the sexes.
5. It has many types of hereditary variations that
can be seen with low power microscope.

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16
Q

linkage

recombination

A

physical association of two genes

generation of non parental gene recombination’s

17
Q

genetic maps

A

alfred sturtevant

frequency of recombination between gene pairs on the same chromosome as a measure of distance between genes and mapped.

18
Q

polygenic traits

example

A

some traits are controlled by three or more genes and are thus called polygenic traits

19
Q

pleiotropy

example

A

it is when a single gene exhibits multiple phenotypic expression

20
Q

mutation

point mutation

A

alteration of DNA and consequently results on changes in the genotype and phenotype of an organism
a change in a a single base pair of DNA

21
Q

pedigree analysis

A

analysis of traits in several generations of a family

22
Q

mendelian disorders

chromosomal disorders

A

alteration or mutation in a single gene

caused due to absence of excess or abnormal arrangement of one or more chromosomes

23
Q
color blindness
haemophilia
sickle cell anaemia
phenylketonuria
thalassemia
A

defect in recognizing red-green. x linked
x linked. clotting of blood is affected
autosome related shape of rbc to sickle shape
autosomal. mental retardation loss of hair and skin pigmentation
autosome. hemoglobin production is affected

24
Q

aneuploidy

polyploidy

A

failure of segregation of chromatids during cell division results in the gain or loss of chromosomes.
failure of cytokinesis after telophase stage of cell division resulting in gain of extra set of chromosomes

25
Q

down syndrome
Klinefelter’s syndrome
turners syndrome

A

presence of an additional copy of the chromosome no 21 trisomy 21
presence of an additional copy of x chromosome
absence of one of the x chromosomes