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In chickens, a key gene involved in sex determination has recently been identified. Called DMRT1, it is located on the Z chromosome and is absent on the W chromosome. Like SRY in humans, it is male determining. Unlike SRY in humans, however, female chickens (ZW) have a single copy while males (ZZ) have two copies of the gene. Nevertheless, it is transcribed onlyin the developing testis. Working in the laboratory of Andrew Sinclair (a co-discoverer of the human SRY gene), Craig Smith and colleagues were able to “knock down” expression of DMRT1 in ZZ embryos using RNA interference techniques (see Chapter 15). In such cases, the developing gonads look more like ovaries than testes [Nature 461: 267 (2009)]. What conclusions can you draw about the role that the DMRT1 gene plays in chickens in contrast to the role the SRY gene plays in humans?
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- Sexual differentiation begins close to 4 weeks after fertilization, but cannot be seen visually until about 6 weeks post fertilization. All fetuses begin with a ______________________ gonad that is able to become either ovaries or testes, depending on the presence or absence of the Y chromosome. If the Y chromosome is present, a region of the Y chromosome will begin expressing genes that start the process of masculinization of internal structures. This region is known as the ______________________________ region or ___________ for short. The expression of these genes causes the bipotential gonad to develop into the testes. Once the testes have started developing, two hormones, testosterone and Anti-MüllerianHormone are produced. Testosterone causes the _____________________ ducts to develop into the _____________________. Testosterone also causes the internal development of the __________________ and __________________. Anti-Müllerian Hormone causes the ______________________ ducts…arrow_forwardIt is estimated that in about 1/150,000 births, an individual is born with 46 chromosomes, both an X and a Y chromosome, but is externally a phenotypic female at birth. A mutation in the gene for which protein is the most likely explanation for this condition? A. Chorionic gonadotropin B. Anti-Müllerian hormone receptor C. Testes determining factor D. Wolffian regression factor (WRF) E. Estrogen receptor βarrow_forwardWhat will be the effect on sexual development in newly fertilized Drosophila embryos if the following genes are deleted? Q. doublesexarrow_forward
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- Which of the following could explain how might a human having the XX sex chromosomes can develop as a male? Both of his X chromosomes become inactivated giving rinse to a male. The autosomal Sox9 gene is inactivated in the male. This is not possible. His father suffered a chromosomal translocation in the reproductive cells that moved the SRY region to the X chromosome. The ratio of X chromosomes to haploid sets of chromosomes has been altered.arrow_forwardIn the process of Oogenesis in animal cells, will the genotype of the second polar body (derived from meiosis II) always be identical to that of the ootid? Why or why not?arrow_forward. Researchers discovered recently that the sole functionof the SRY protein is to activate an autosomal genecalled Sox9 in the presumptive gonad (before it has“decided” to become a testis or an ovary).a. What would be the sex of an XY individual homozygous for nonfunctional mutant alleles of Sox9?Explain.arrow_forward
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