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Related Concept Videos

X-Inactivation01:58

X-Inactivation

The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, one might expect females to produce twice as many of the proteins, with undesirable results.
Renewal of Intestinal Stem Cells01:23

Renewal of Intestinal Stem Cells

The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the goblet,...

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Isolation and Th17 Differentiation of Na&iuml;ve CD4 T Lymphocytes
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A quantitative trait locus on chr.4 regulates thymic involution.

Ritu Kumar1, Serine Avagyan, Hans-Willem Snoeck

  • 1Department of Gene and Cell Medicine, Mount Sinai of School of Medicine, Gustave L. Levy Place, PO Box 1496, New York, NY 10029, USA.

The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|April 8, 2010
PubMed
Summary
This summary is machine-generated.

Scientists identified a gene region on mouse chromosome 4 that significantly impacts thymic involution, the aging of the thymus. This discovery offers new insights into the genetic regulation of this crucial immune aging process.

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Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization

Published on: February 3, 2013

Area of Science:

  • Immunology
  • Genetics
  • Aging Research

Background:

  • Age-associated thymic involution, a decline in thymus function with age, lacks understood mechanisms.
  • Genetic variation between mouse strains influences thymic involution.
  • Identifying genes involved could illuminate the process of immune aging.

Purpose of the Study:

  • To investigate the hypothesis that a quantitative trait locus (QTL) on mouse chromosome 4 regulates thymic involution.
  • To identify genetic factors contributing to age-related thymus shrinkage.

Main Methods:

  • Utilized B6.D2-chr.4 congenic mice, which possess a specific region of chromosome 4 introgressed from DBA/2 mice into a C57BL/6 background.
  • Compared thymus size and the maintenance of early thymic precursors in aged congenic mice versus aged C57BL/6 control mice.

Main Results:

  • Aged B6.D2-chr.4 congenic mice exhibited larger thymi compared to aged C57BL/6 controls.
  • Congenic mice showed better preservation of early thymic precursors.
  • These findings pinpoint a QTL on the telomeric region of chromosome 4, designated Ti1 (thymic involution 1), as a regulator of thymic involution.

Conclusions:

  • The telomeric region of mouse chromosome 4 contains a significant QTL (Ti1) that regulates thymic involution.
  • The identified QTL (Ti1) may be identical to Tb2r1, a previously identified QTL regulating hematopoietic stem and progenitor cell responsiveness to TGF-beta 2.
  • This research provides a key genetic locus for understanding and potentially intervening in thymus aging.