Koo Dal-Hoe, Sehgal Sunish K, Friebe Bernd, Gill Bikram S
Department of Plant Pathology, Wheat Genetics Resource Center, Throckmorton Plant Sciences Center, Kansas State University, Manhattan, KS, 66506-5502, United States of America.
Department of Plant Science, South Dakota State University, Brookings, SD, 57007, United States of America.
PLoS One. 2015 Sep 18;10(9):e0137747. doi: 10.1371/journal.pone.0137747. eCollection 2015.
In most eukaryotes, centromeres assemble at a single location per chromosome. Naturally occurring telocentric chromosomes (telosomes) with a terminal centromere are rare but do exist. Telosomes arise through misdivision of centromeres in normal chromosomes, and their cytological stability depends on the structure of their kinetochores. The instability of telosomes may be attributed to the relative centromere size and the degree of completeness of their kinetochore. Here we test this hypothesis by analyzing the cytogenetic structure of wheat telosomes. We used a population of 80 telosomes arising from the misdivision of the 21 chromosomes of wheat that have shown stable inheritance over many generations. We analyzed centromere size by probing with the centromere-specific histone H3 variant, CENH3. Comparing the signal intensity for CENH3 between the intact chromosome and derived telosomes showed that the telosomes had approximately half the signal intensity compared to that of normal chromosomes. Immunofluorescence of CENH3 in a wheat stock with 28 telosomes revealed that none of the telosomes received a complete CENH3 domain. Some of the telosomes lacked centromere specific retrotransposons of wheat in the CENH3 domain, indicating that the stability of telosomes depends on the presence of CENH3 chromatin and not on the presence of CRW repeats. In addition to providing evidence for centromere shift, we also observed chromosomal aberrations including inversions and deletions in the short arm telosomes of double ditelosomic 1D and 6D stocks. The role of centromere-flanking, pericentromeric heterochromatin in mitosis is discussed with respect to genome/chromosome integrity.
在大多数真核生物中,每条染色体的着丝粒在单一位置组装。具有末端着丝粒的天然端着丝粒染色体(端体)很罕见,但确实存在。端体通过正常染色体着丝粒的错误分裂产生,其细胞学稳定性取决于动粒的结构。端体的不稳定性可能归因于相对着丝粒大小及其动粒的完整程度。在这里,我们通过分析小麦端体的细胞遗传学结构来检验这一假设。我们使用了由小麦21条染色体错误分裂产生的80个端体群体,这些端体在许多代中都表现出稳定的遗传。我们用着丝粒特异性组蛋白H3变体CENH3进行探针检测来分析着丝粒大小。比较完整染色体和衍生端体之间CENH3的信号强度表明,端体的信号强度约为正常染色体的一半。对含有28个端体的小麦品系进行CENH3免疫荧光检测发现,没有一个端体获得完整的CENH3结构域。一些端体在CENH3结构域中缺乏小麦着丝粒特异性逆转座子,这表明端体的稳定性取决于CENH3染色质的存在,而不是CRW重复序列的存在。除了为着丝粒移位提供证据外,我们还在双端体1D和6D品系的短臂端体中观察到包括倒位和缺失在内的染色体畸变。我们讨论了着丝粒侧翼的着丝粒周围异染色质在有丝分裂中对基因组/染色体完整性的作用。