𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Genetic conflict and evolution of mammalian X-chromosome inactivation

✍ Scribed by Moore, Tom ;Hurst, Laurence D. ;Reik, Wolf


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
678 KB
Volume
17
Category
Article
ISSN
0192-253X

No coin nor oath required. For personal study only.

✦ Synopsis


The existence of parentally imprinted gene expression in the somatic tissues of mammals and plants can be explained by a theory of intragenomic genetic conflict, which is a logical extension of classical parent-offspring conflict theory. This theory unites conceptually the phenomena of autosomal imprinting and X-chromosome inactivation. We argue that recent experimental studies of X-chromosome inactivation and androgenetic development address previously published predictions of the conflict theory, and we discuss possible explanations for the occurrence of random X-inactivation in the somatic tissues of eutherians. o 1995 WiIey-Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Genetic significance of skewed X-chromos
✍ Sato, Kazuyo ;Uehara, Shigeki ;Hashiyada, Masaki ;Nabeshima, Hiroshi ;Sugawara, πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 124 KB πŸ‘ 1 views

## Abstract To determine the relationship between premature ovarian failure (POF) and skewed X‐chromosome inactivation (XCI), karyotype, and XCI status in 43 patients with POF (group I) and 43 age‐matched control women with regular menstrual cycles (group II) were evaluated. Evaluation of XCI statu

Evolution of the mammalian Y chromosome
✍ Graves, Jennifer A. Marshall πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 131 KB πŸ‘ 2 views

In mammals, male sex determination, as well as spermatogenesis, is controlled by genes on the Y chromosome. Evolutionary comparisons may be used to detect and test candidate genes for these functions, under the hypothesis that the rapid evolution of the mammalian Y chromosome causes it to contain fe

XIST and the mapping of the X chromosome
✍ Stephen D. M. Brown πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 746 KB

## Location of an X-inactivation Centre in Mouse and Human Experiments utilising X-autosome translocations in or autosomal insertions into X chromosome material(") indicated that autosomal coat colour genes placed adjacent to X chromosome material could be inactivated resulting in coat colour vari

Analysis of X chromosome inactivation in
✍ Xiaohong Gong; Elena Bacchelli; Francesca Blasi; Claudio Toma; Catalina Betancur πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 114 KB πŸ‘ 2 views

## Abstract Autism spectrum disorders (ASD) are complex genetic disorders more frequently observed in males. Skewed X chromosome inactivation (XCI) is observed in heterozygous females carrying gene mutations involved in several X‐linked syndromes. In this study, we aimed to estimate the role of X‐l

LοΏ½ri-Weill syndrome associated with a ps
✍ Baralle, D. ;Willatt, L.R. ;Shears, D.J. πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 168 KB πŸ‘ 2 views

A female patient of normal intelligence with short stature and Madelung deformity is reported with Le Β΄ri-Weill dyschondrosteosis and a de novo pseudodicentric X;Y translocation chromosome. The phenotype is consistent with the observed deletion of the SHOX gene by FISH and molecular studies. The Y c