Related Experiment Video
Updated: Jul 28, 2026

10:11
Using Quantitative Real-time PCR to Determine Donor Cell Engraftment in a Competitive Murine Bone Marrow Transplantation Model
Published on: March 7, 2013
Genotypic analysis using a Y-chromosome-specific probe following bone marrow transplantation
H Morisaki1, T Morisaki, Y Nakahori
1Department of Pathological Pharmacology, University of Tokyo, Japan.
American Journal of Hematology
|January 1, 1988
Summary
A Y-chromosome-specific DNA probe (pHY10) offers a sensitive and rapid method for monitoring bone marrow transplant engraftment. This technique effectively confirms donor cell engraftment and detects mixed chimerism in peripheral blood and bone marrow post-transplantation.
Area of Science:
- * Molecular Biology
- * Genetics
- * Hematology
Background:
- * Bone marrow transplantation (BMT) is a critical therapy for various hematologic disorders.
- * Monitoring successful engraftment of donor cells is essential for therapeutic success.
- * Current monitoring methods can be time-consuming or lack sensitivity.
Observation:
- * Southern hybridization and dot blot analyses were employed using a Y-chromosome-specific DNA probe (pHY10).
- * This probe targets the Y-chromosome, enabling sex-mismatched monitoring.
- * The DNA probe facilitated rapid and sensitive detection of Y-chromosomal DNA.
Findings:
- * The pHY10 probe demonstrated high sensitivity and speed in identifying Y-chromosome-containing cells.
- * Post-transplantation analysis of peripheral blood and bone marrow confirmed engraftment.
- * The method successfully detected mixed lymphohematopoietic chimerism.
Implications:
- * This Y-chromosome probe provides a valuable tool for routine monitoring of BMT engraftment.
- * It aids in early detection of engraftment failure or mixed chimerism.
- * Enhanced monitoring can lead to timely therapeutic adjustments and improved patient outcomes.
Related Concept Videos
Pedigree Analysis
Overview
Karyotyping
Describing the number and physical features of chromosomes can reveal abnormalities that underlie genetic diseases. This description is facilitated by special staining techniques that produce a particular banding pattern on each chromosome. State-of-the-art techniques make this approach even more powerful, enabling the detection of individual genes that cause disease.A Simple Chromosome Staining Technique Provides Valuable Scientific InsightSome genetic diseases can be detected by looking at...
The Y Chromosome Determines Maleness
The Y chromosome is a sex chromosome found in several vertebrates and mammals, including humans. In addition to 22 pairs of autosomes, the human males have one X chromosome and one Y chromosome. In these organisms, the presence or absence of the Y chromosome determines the development of male traits.
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size. Today,...
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size. Today,...
Bone Marrow Sampling and Transplants
Bone marrow transplant is a potential cure for several diseases, including cancer and specific genetic disorders. Notably, this procedure is applicable for patients suffering from aplastic anemia, certain types of leukemia, severe combined immunodeficiency disease (SCID), Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, thalassemia, sickle-cell disease, and certain cancers.
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy the...
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy the...

