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hereditary
science that deals with the principles of how characters are transmitted from parent to offspring
reason for mendel using garden pea
PISCUM SATIVUM is used because
-short life span
self fertilisation can be controlled
large number of contrasting characters
structurally suitable for cross pollination
bisexual
reasons for mendels success
utmost care
took notes and analysed statistically
emasculation and bagging to prevent self pollination
started experiments with pure line character plants
kept plants with different characters separately to prevent intermingling
monohybrid cross explanation
pure line cross pollination, show diagram
conclusion- disappearance of dwrf in f1 but the reappearence in F2 formed mendles law of dominance
alleles
each genetic character is governed by factors called alleles
law of dominance
Flashcard:
Term: Law of Dominance
Definition: In geneticsthe law states that when two different alleles are present in an organism, one allele can mask the expression of the other, resulting in the dominant trait being expressed in the phenotype.
the character that appears in F1 generation is
DOMINANT
law of segregation
Flashcard Term: Law of Segregation
Definition: The principle stating that during the formation of gametes, the two alleles for a trait separate so that each gamete carries only one allele for each gene. This means that offspring inherit one allele from each parent, ensuring genetic diversity.
from a pair of contrasting characters only one is present in a single gamete , and one character is dominant and other is recessive in F1 AND F2 these characters are segregated in the ration 3:1
what helped mendel create law of dominance and segregation
MONOHYBRID CROSS
genotype
genetic makeup
phenotype
Term: Phenotype
Definition: The observable physical and physiological traits of an organism
conclusion of dihybrid cross
the genetic inheritance of two contrasting characters in independant of each other, the genes for two characters do not influence each other
MODIFICATION- as long as they are present on different homologous chromosomes.
law of independent assortment
when there are two pairs of contrasting characters the distribution of each pair to a gamete is independent to the distribution of the other pair of characters
test cross does what
determines genetic nature of an individual
dominant phenotype may be homozygous or heterozygous
in test cross can dominant phenotype be hetero or homo
BOTh
test cross working
unknown geneotypes are crossed with HOMOZYGOUS RECESSIVE
if reslults of test cross show all dominant phenotypes ( homo and hetero)
the geneotype is HOMOZYGOUS DOMINANT
if results show equal dominant and recessive phenotypic ratio
HETEROZYGOUS DOMINANT
no of gemetes
2 to the power n
( n= heterozygous pairs )
no of phenotypes in selfing F2
2 to the power n
no of genotypes in selfing F2
3 to the power n
no of zygotes formed from F2 selfing
4 TO THE POWER N
biological imp of mendels laws
plant breeders- to produce crops with desirable characters
animal breeders to promote quality cattle and poultry
remove defective characters from the human race and promote useful genes in the human population
laif the foundation for modern molecular genetics
incomplete dominance
SNAP DRAGON
pure red and pure white flowers crossed whoch in F1 gave all pink flowers goes against mendels first principle,
IN f2 RATIO was 1:2:1 which goes against law 2
in incomplete dominance , domiance is not perfect or complete , alleles interact with one another which causes causes bleeding characteristics
codominace
Flashcard:
Term: Codominance
Definition: A genetic scenario in which both alleles in a heterozygous organism are fully expressed, resulting in a phenotype that displays characteristics of both alleles.
BLOOD GROUP a and b when separate show separately but together in heterozygous ( present in same allele) become BLOOD GROUO AB
homozygous parent produces gametes that are
SIMILAR
multiple alleles
Front:What is a genetic scenario involving more than two alternative forms of a gene?
Back:This concept refers to a situation where a single gene has more than two possible alleles, leading to a variety of phenotypes. Common examples include blood type in humans,
inheitance of abo blood group
goverened by 3 alleles Ia Ib and i
IA IB and i result in
4 blood groups
A,B ,AB AND O
IA AND IB ARE
codominant
i allele is
recessive to both IA AND IB
geneotypes for A,B, AB AND O
IA IA, IA i
IB IB , IB i
IA IB
ii
no . of genotypes when allele is given
n(n+1)/2
n= alleles
PLEIOTROPIC GENE
when one gence influences the expression of more than one character
pku
phenylketonuria
mutation in the gene coding for enzyme phenlyalanine hydroxylase.
enzyme phenylallanine hydroxylase converts phenylalanine to tryrosine.
in absence of this enzyme- phenylallanine accumulates in blood and results in mental retardation
tyrosine precursor to melanin so with the mutation melanin cannot be synthasised= albinism
starch synthesis as an example of pleitropy
one gene is controlled by two alleles - B and b
gene B is used to dteremine both shape and size see book page 189
mullato
intermediate skin colour
polygenic inheritance
quantity of genes determine nature of inheritance
chromosomal theory of inheritance
parallelism between gene and chromosomes
both are found in pairs
both are separated after gametogenesis
both return to their paired state after fertilisation
features of chromosomal theory
after fertilistaion diploid zygote is formed , this zygote containeschromosomes shares by maternal and paternal parent, zygote get a chromosome of the each type from both set of parents , this set of both = HOMOLOGOUS CHROMOSOME
during gamete formation g=homolgous chromosome is separated therefore gene is also separated
each chromosome carries genes
chromosomes remain unique and structurally unique throughoutr outr lives
why did morgan use fruit flies
good sexual dimorphism
short life span
one mating mutiple offspring
recognisable clear cut characters
allosome
FlashcardDefinition: A type of chromosome that determines the sex of an organism, differing in shape or size between sexes. In humans, these are the X and Y chromosomes, with females typically having two of the same kind and males having one of each. They play a crucial role in sexual reproduction and inheritance patterns.
autosome
chromosomes other than sex chromosome 22 pairs
sex determination
determining sex
homogametic female sex determination
grass hopper 2A+ XX AND 2A+XO
human 2A+ XX AND 2A + XY
homogametic male
birds 2A+ZW AND 2A+ZZ
SEX DETERMINATION IN HINEY BEE
VERY IMPORTANT
linkage
genes that are together during the course of inheritance
significance of linkage
preserves parental traits
reduces variability
gene location
prevents recombination
crossing over and significance
exchange of chromosomal parts between non sister chromatids or homologous chromosomes
variation
chromosomal maps
genes linear manner
evolution
chromosomal abberations
affect number and structure of chromosomes
euploidy
monoploidy
polyploidy
autoplooidy
allopolyploids
autoalloploidyploids
colour blindness for blue colour is
AUTOSOMAL
red , green, blue blindness names
protanopia , beuteranopia tritanopia
klinefelters, turners , down syndrome
2a+ XXY , 2A+ XO , 21ST trisomy
hameophilia more likely in males
x linked femals have two , chnaces of both being affected are lessers