The House Fly Y Chromosome is Young and Undifferentiated from its Ancient X Chromosome Partner
نویسندگان
چکیده
Ancient or canonical sex chromosome pairs consist of a gene rich X (or Z) chromosome and a male(or female-) limited Y (or W) chromosome that is gene poor. In contrast to highly differentiated sex chromosomes, nascent sex chromosome pairs are homomorphic or very similar in sequence content. Nascent sex chromosomes arise frequently over the course of evolution, as evidenced by differences in sex chromosomes between closely related species and sex chromosome polymorphisms within species. Sex chromosome turnover typically occurs when an existing sex chromosome becomes fused to an autosome or an autosome acquires a new sex-determining locus/allele. Previously documented sex chromosome transitions involve changes to both members of the sex chromosome pair (X and Y, or Z and W). The house fly has sex chromosomes that resembles the ancestral fly karyotype that originated 100 million years ago, and therefore house fly is expected to have differentiated X and Y chromosomes. We tested this hypothesis using whole genome sequencing and transcriptomic data, and we surprisingly discovered little evidence for X-Y differentiation in house fly. We propose that house fly has retained the ancient X chromosome, but the ancestral Y was replaced by an X chromosome carrying a male determining gene. In this evolutionary scenario, the house fly has an ancient X chromosome that is partnered with with a neo-Y chromosome. This example of sex chromosome recycling illustrates how one member of a sex chromosome pair can experience evolutionary turnover while the other member remains unaffected. 2 . CC-BY-NC-ND 4.0 International license peer-reviewed) is the author/funder. It is made available under a The copyright holder for this preprint (which was not . http://dx.doi.org/10.1101/073023 doi: bioRxiv preprint first posted online Sep. 1, 2016;
منابع مشابه
The house fly Y Chromosome is young and minimally differentiated from its ancient X Chromosome partner.
Canonical ancient sex chromosome pairs consist of a gene rich X (or Z) Chromosome and a male-limited (or female-limited) Y (or W) Chromosome that is gene poor. In contrast to highly differentiated sex chromosomes, nascent sex chromosome pairs are homomorphic or very similar in sequence content. Nascent sex chromosomes can arise if an existing sex chromosome fuses to an autosome or an autosome a...
متن کاملO-7: Y Chromosome Microdeletions Are Not Associated with Spontaneous Recurrent Pregnancy Loss in A Sinhalese Population in Sri Lanka
Background: Many advances have been made in reproductive medicine yet the spontaneous loss of a pregnancy remains the most common complication of pregnancy. The aetiology of spontaneous recurrent pregnancy loss (RPL) is multifactorial. Y chromosome microdeletions are found in approximately 7% of men with low sperm counts and, compared to the general population, a higher frequency of spontaneous...
متن کامل-
The homeobox genes are known to play a crucial role in controlling the development of multicellular organisms. The majority of these genes have been determined to express regulatory proteins act as a regulatory protein. These trans-acting factors regulate the expression of proteins that are necessary during the developmental processes throughout the body. TGIFLX/Y is a homeobox gene and it cont...
متن کاملCHROMOSOME STUDIES OF IRANIAN MEMBERS OF TRIBE SOPHOREAE (FAMILY LEGUMINOSAE
The tribe Sophoreae sensu Polhill [9,10] is a large and diverse assemblage comprising the ancient and primitive ancestral stocks of Papilionoideae. The most frequent chromosome basic numbers in this tribe are x = 11 and x = 9 but chromosome numbers range from x = 8-14 are also known. In this study chromosome numbers and karyotype variation of Iranian members of tribe Sophoreae are reported. Ira...
متن کاملبررسی ارتباط میان ریزحذفهای کامل کروموزوم Y و وقوع سقط مکرر در جمعیت ایرانی
Background: Recurrent pregnancy loss is a form of infertility with at least three consecutive pregnancy losses or more. Y chromosome microdeletions are a class of most likely genetic factors that occur in a special zone of Y chromosome which is named azoospermia factor region. The purpose of this study was to analyze the presence of Y chromosome complete microdeletions in male partner of couple...
متن کامل