1) SRY gene on the X chromosome is responsible for the development of male reproductive organs, the genotype of normal males is XY and genotype of normal females is XX, that is females do not have Y chromosome, if the SRY gene is translocated to another chromosome, and if the female progeny gets that chromosome with the SRY region, then female develops male reproductive organs so the answer is translocation of SRY to the autosome of a 46,XX
2) the maximum possible recombination frequency is 50%,
let's consider 2 genes A and B located on a different chromosome
the dihybrid was obtained by the cross between AABB and aabb
so in the dihybrid the alleles A and B are on one chromosome and alleles a and b are on another chromosome, so AB and ab are parental type gametes and aB and Ab are recombinant type gametes
the dihybrid AaBb is crossed to aabb
AaBb* aabb
| AB | aB | Ab | ab | |
| ab | AaBb (parental type) | aaBb (recombinant) | Aabb(recombinant) | aabb(parental type) |
if the genes are on the different chromosome ( or the genes are not linked that is far apart in a chromosome ) then we expect each class of progeny in equal proportions so
the number of recombinant progenies = number of parental type progenies
recombination frequency= (number of recombinant progenies/total
number of progenies )100
=(2/4)100
that is if the recombination frequency between 2 genes is 50% then the genes are not linked
so the answer is the two genes are likely to be located on different chromosomes.
Question 1 1 pts Sex determination in mammals is due to the SRY region of the...
15. What will be the phenotypic sex of a human with the following gene or chromosomes or both? a. XY with the SRY gene deleted + b. XY with the SRY gene located on an autosomal chromosome c. XX with a copy of SRY gene on an autosomal chromosome M d. XO with a copy of SRY gene on an autosome M e. XXY with the SRY gene deleted F f. XXYY with one copy of the SRY gene delete...
Match each phenotype description to its corresponding sex chromosome genotype in humans. XY with SRY deleted XXX XXY XYY XO with SRY on an autosome phenotypically male but karyotype indicates presence of only X chromosome Answer Bank phenotypically female but karyotype indicates presence of both sex chromosomes phenotypically male with an increase in average stature phenotypically female with some abnormalities and overexpression of X chromosome genes phenotypically male with sterility and hypogonadism
The sex-determining region in mammals is called the and is located on the v chromosome. QUESTION 24 The sex-determining region in mammals is called the < and is located on the chromosome SRY gene QUESTION 25 SLY gene X Which of the following structures would you expect to of a cell with a previously existing reciprocal balanced Y
Aneuploidy of an autosome is always more harmful than an aneuploidy of a sex chromosome. One of the explanations as to why sex-chromosome aneuploids are less harmful is due to X inactivation. X-inactivation assures that all human cells only express a single X chromosome regardless of how many X chromosomes are present. Interestingly, sex chromosome aneuploids (i.e. XXY, XO) still have some different phenotypes compared to either an XX or XY individual. For instance, XXY individuals (Klinefelter Syndrome) are taller, have...
1. Animals can teach us genetics. Match Codominance Show a dominant and recessive relationship _An allelic series A dominant homozygote is lethal Coat coloration is determined by 2 genes Shows variable expressivity A qualitative, or continuous, trait involving polygenes Females mosaics for X-linked heterozygous color genes A. Manx cat B. Coat coloration rabbits C. Labrador retriever dogs D. Piebald spotting in beagles E. A and B blood alleles F. A and O blood alleles G. Calico cat H. Height of...
I need answers for 5 to 8. thank you
5. It is probable that a probability question is in the future From the cross AaBbceDdEell X AABECcDdeer what is the probability of obtaining the genotype AabbCcDDEeff in the progeny? 6. Fill in XY female Cri du Chat Down syndrome XX male Anhydrotic ectodermal dysplasia Patau syndrome Hemophilia Polydactyly Phenylketonuria Achondroplasia Alkaptonuria a) Develop male structure, but experiences infertility b) Develop female structures but may not have ovaries c) Female heterozygotes...
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
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Nameindulia Los Drosophila Genetics Predictions-L113 (20 pts.) Part I. Meiosis and Punnett Squares Remember, whenever you use Punnett Squares to solve genetics problems, be sure you are completing each of the following steps: 1) Identify the genotypes of the parents. 2) For the specific traits of interest, figure out what kinds of haploid gametes each parent can make. In each gamete, there should be one allele for each trait of interest. If there is more than one trait, make sure...
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