cromossomal

Cromossomal, also written chromosomal in English, is an adjective used in genetics to describe anything related to chromosomes, the thread-like structures in cells that carry DNA and genes. In humans, somatic cells typically contain 46 chromosomes, arranged in 23 pairs (22 autosomes and 1 pair of sex chromosomes).

Chromosomes exist as compact units of chromatin, formed by DNA wrapped around histone proteins. Each chromosome has a centromere, which serves as the attachment point for sister chromatids during cell division, and telomeres at the ends that protect the chromosome from degradation. During replication, each chromosome is copied to produce two sister chromatids that separate during mitosis or meiosis.

Chromosomal abnormalities affect structure or number of chromosomes. Numerical abnormalities include aneuploidy, such as trisomies or monosomies. Structural abnormalities involve deletions, duplications, inversions, translocations, or more complex rearrangements. These changes can disrupt gene dosage or create abnormal gene fusions, contributing to congenital disorders or cancer. Examples include Down syndrome (Trisomy 21), Turner syndrome (Monosomy X), and the Philadelphia chromosome translocation t(9;22) associated with chronic myelogenous leukemia.

Detection and characterization of chromosomal changes use cytogenetic and molecular techniques, including karyotyping, fluorescence in situ hybridization (FISH), microarray-based comparative genomic hybridization (array CGH), and DNA sequencing. These tools are used in clinical genetics for diagnosis, prognosis, and prenatal screening.

Chromosomal integrity is essential for proper gene dosage and development, and rearrangements can influence evolution through changes in genome structure and gene regulation.