MCDB 4650 Dosage Compensation. Which of the following is true of a worm that is homozygous mutant for xol-1 (lf)--one of the dosage compensation genes?

Slides:



Advertisements
Similar presentations
General Genetics Ayesha M. Khan Spring 2013.
Advertisements

X-inactivation 20/11/08.
Patterns of Chromosome Inheritance
Studying Segmentation Mutants in Balanced Stocks.
MCDB 4650 Developmental Genetics in Drosophila
MATTERS OF SEX Anueploidy Monosomy
Urogenital Development II & Sex Determination
Inheritance Patterns Related to Gender Determination
CHAPTER 15 THE CHROMOSOMAL BASIS OF INHERITANCE Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings Section B: Sex Chromosomes 1.The.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
KEY CONCEPT Phenotype is affected by many different factors.
Central Dogma of Molecular Biology
14.21 General scheme of development in the vertebrate kidney (Part 1)
Genetics of Sex Sex Determination Evolution of Sex Chromosomes
Developmental Genetics, I.How do different cell types become organized into tissues, organs & systems? II.Sex determination in Drosophila III.Sex determination.
Sex Determination in Humans
X-inactivation. Males are haploid for X-linked genes.
Chromosomal Inheritance, Sex Linkage, & Sex Determination:
The Hunt for Chromosomal Determinants of Maleness— A gene mapping story……. The Hunt for Chromosomal Determinants of Maleness— A gene mapping story…….
SEX DETERMINATION.
Inheritance of Sex and Sex-Linked or Influenced Traits.
The Chromosomal Basis of Inheritance Chapter 15. The Chromosomal Theory of Inheritance chromosomes and genes are present as pairs in diploid cells homologous.
Influence of Sex on Genetics Chapter Six. Humans 23 Autosomes –Chromosomal abnormalities very severe –Often fatal All have at least one X –Deletion of.
Sex Determination and Sex-Linked Characteristics
Sex = Sum total of those differences in structure and function on the basis of which an organism is classified as male or female. Theories of sex determination:
Sex Determination and Sex Chromosomes
Objective 10: TSWBAT explain the chromosomal basis of sex and the unique inheritance patterns of sex-linked genes.
Sex Determination. Sexual Reproduction For most diploid eukaryotes, sexual reproduction is the only mechanism resulting in new members of a species. Meiosis.
LECTURE CONNECTIONS 4 | Sex Determination and Sex-Linked © 2009 W. H. Freeman and Company Characteristics.
The X and Y Chromosomes. From a comparison of the genes on the X and Y chromosomes, we can infer that, even though the X is now much larger than the Y,
LECTURE CONNECTIONS 4 | Sex Determination and Sex-Linked © 2009 W. H. Freeman and Company Characteristics.
Sex Determination.
7.1 Chromosomes and Phenotype KEY CONCEPT The chromosomes on which genes are located can affect the expression of traits.
LECTURE – 4 Learning objectives 1. Sex chromosome disorders 2. Sexual ambiguity 3. Chromosomal instability syndromes.
A second practice problem set (with answers) is on the course website. The review session for the second midterm is on Thursday evening, April 10, from.
7.1 Chromosomes and Phenotype KEY CONCEPT The chromosomes on which genes are located can affect the expression of traits.
Intermediate Mesoderm: Kidney and Gonad Development Gilbert: Chapter 14, 17.
Ch.6: Sexual Identity Genetics. Males (XY) are the heterogametic sex. Females (XX) are homogametic sex. X chromosome has over 1,000 genes. Y chromosome.
Chromosomal Mutations Entire chromosomes extra or missing Pieces of chromosome missing or moved onto a different chromosome. Identified by Karyotypes.
X inactivation and Practice Questions
Sex Determination.
Two copies of each autosomal gene affect phenotype.
7.1 Chromosome and Phenotype
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
The great variety of possible gene combinations in a
Mendel’s Genetics Chapter 7.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Chromosomal Mutations
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Development: Cell Division, Cell Differentiation, and Morphogenesis
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Gene control mechanisms may interact with ________.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
7.1 Chromosomes and Phenotype
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Two copies of each autosomal gene affect phenotype.
Presentation transcript:

MCDB 4650 Dosage Compensation

Which of the following is true of a worm that is homozygous mutant for xol-1 (lf)--one of the dosage compensation genes? a.XX embryos develop into male worms b.XO embryos develop into hermaphrodite worms c.XO embryos die due to lack of X chromosome gene products d.XX embryos die due to overproduction of X chromosome gene products

If they could survive, the xol-1 mutant XO animals would have a: a.Male gonad b.Hermaphrodite gonad c.Something in between d.No gonad

Now think about Drosophila. In which chromosomal combination would a loss of function mutation in the Sxl (sex lethal) gene be lethal? a.XX b.XY c.Neither d.Both

You are doing chromosomal analysis of an individual with two X chromosomes who appears externally male. You find that one of the X chromosomes contains a large translocation from the Y chromosome, containing the SRY gene. If you were able to look at multiple tissue samples from this individual’s gonad, you would expect to see: a.The gonadal cells have all differentiated into testis tissue b.The gonadal cells have all differentiated into ovarian tissue c.The gonadal cells have not differentiated into testis or ovarian tissue d.Some gonadal cells have differentiated into testis, some into ovarian tissue

Say there are approximately equal amounts of testicular and ovarian tissue in the gonad from the previous example. What characteristics would this person have? a. ductal system male, external male secondary sex characteristics b. ductal system male, external female secondary sex characteristics c. ductal system female, external female secondary sex characteristics d. ductal system female, external male secondary sex characteristics

Individuals with an XXY genotype are infertile because: a.Testes do not develop normally b.Cannot produce testosterone c.Cannot respond to AMH d.Extra X transcripts interfere with male fertility

If an XY individual contained an extra copy of the Xist region, translocated onto an autosome, what would happen? a.Their X chromosome would be inactivated b.The autosome with the Xist region would be inactivated c.The autosome would be inactivated sometimes; the X inactivated sometimes d.Neither would be inactivated, because there’s still only one X chromosome

How can both male and female mammals undergo normal development when they have different numbers of X chromosomes? a. Males need fewer of the X chromosome gene products than females. b. Both males and females only need one copy of most X chromosome genes. c. Genes on the X chromosome are activated differently in males and females. d. Males and females have different genes on their X chromosomes.

True/false. C. elegans and Drosophila use the same basic mechanism for dosage compensation, but differ as to which sex upregulates or downregulates the X chromosome.

True/false. Mammalian dosage compensation is controlled by the same genetic pathway as sex determination

True/false. Xist is primarily transcribed from the X chromosome that will be active.

A homozygous lf mutation in the dosage compensation gene sdc-2 will kill otherwise normal hermaphrodite but not male embryos. Consider double mutant embryos of the following four genotypes and phenotypes. Which two of them will die? a. sdc-2(0); tra-1(0) XX (male gonad) b. sdc-2(0); tra-1(0) XO (male gonad) c. sdc-2(0); her-1(0) XX (hermaphrodite gonad) d. sdc-2(0); her-1(0) XO (hermaphrodite gonad)

Suppose that an XX individual is heterozygous for a loss of function mutation in Xist. What result would you expect regarding X inactivation? a.Both X chromosomes are active b.Both X chromosomes are inactive c.X inactivation occurs non-randomly, on the chromosome with the Xist mutation d.X inactivation occurs non-randomly, on the wild type chromosome e.There is no effect on the inactivation of the X chromosomes