๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Characterization of the Xp21-23 region in the wood lemming, a region involved in XY sex reversal

โœ Scribed by Liu, Wan-Sheng ;Nordqvist, Katarina ;Lau, Yun-Fai Chris ;Fredga, Karl


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
293 KB
Volume
290
Category
Article
ISSN
0022-104X

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

The wood lemming (Myopus schisticolor) harbors two types of X chromosome, a normal X and a variant X, designated X*. The X* chromosome contains a mutation that causes XY sex reversal. We have previously demonstrated that the Xp21โ€“23 region is deleted from X* and is associated with XY sex reversal. To further analyze the deleted region, we have constructed and characterized seven X chromosomeโ€ and regionโ€specific recombinant DNA libraries. Further, we have screened mouse fetal gonad cDNA libraries with the microdissected Xp21โ€“23 DNA as a probe in an attempt to identify homologous and expressed sequences from the deletion. Fourteen positive clones were isolated, and sequence analyses showed that ten of these contained identical sequences homologous to mouse ฮณโ€satellite sequences. One of the remaining four was perfectly homologous to the mouse gene Ccth (chaperonin containing tโ€complex polypeptide 1, ฮท subunit). Southern blot indicated that the Ccth cDNA was located on the X chromosome, not deleted from the X* but closely linked to the deletion region. Although the role of the Ccth containing region in sex determination of the wood lemming requires additional studies, the isolation of the mouse Ccth gene by the deletion Xp21โ€“23 probe could be important since this gene is mainly expressed in testis. J. Exp. Zool. 290:551โ€“557, 2001. ยฉ 2001 Wileyโ€Liss, Inc.


๐Ÿ“œ SIMILAR VOLUMES


Major role for a 3p21 region and lack of
โœ Anke van den Berg; Miriam M. F. Hulsbeek; Debora de Jong; Klaas Kok; Patrick M. ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 792 KB

In a loss of heterozygosity analysis of 3p, we examined 44 sporadic cases of renal cell carcinoma (RCC) and matched normal tissue with 18 markers distributed over the whole p-arm. The majority of these markers clustered in three regions that have been suggested t o be involved in the development of

Long-range mapping of the 11q23 region i
โœ Dr. Yukihiro Akao; Yoshihide Tsujimoto; Masao Seto; Takashi Imai; Dominique Berg ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 448 KB

## Abstract We have previously demonstrated that the __RCK__ gene involved in t(11;14)(q23;q32) and the more centromeric __MLL/ALL1__ gene involved in t(4;11)(q21;q23) and t(11;19)(q23;p13) are localized on different adjacent Notl fragments by using pulsedโ€field gel electrophoresis (PFGE) analysis

Expression of p16INK4A and alterations o
โœ George Mariatos; Vassilis G. Gorgoulis; Panayotis Zacharatos; Athanassios Kotsin ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 286 KB ๐Ÿ‘ 1 views

The 9p21-23 chromosome region harbors a number of known and putative tumor-suppressor genes (TSGs). The best characterized gene in this area is p16 INK4A (CDKN2A). Alterations of its product have been observed in various malignancies, including non-small-cell lung carcinomas (NSCLCs). We earlier inv