|
|
|
|
| LEADER |
01000caa a22002652c 4500 |
| 001 |
NLM249754347 |
| 003 |
DE-627 |
| 005 |
20250218154039.0 |
| 007 |
cr uuu---uuuuu |
| 008 |
231224s2015 xx |||||o 00| ||eng c |
| 024 |
7 |
|
|a 10.1111/nph.13497
|2 doi
|
| 028 |
5 |
2 |
|a pubmed25n0832.xml
|
| 035 |
|
|
|a (DE-627)NLM249754347
|
| 035 |
|
|
|a (NLM)26053356
|
| 040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
| 041 |
|
|
|a eng
|
| 100 |
1 |
|
|a Charlesworth, Deborah
|e verfasserin
|4 aut
|
| 245 |
1 |
0 |
|a Plant contributions to our understanding of sex chromosome evolution
|
| 264 |
|
1 |
|c 2015
|
| 336 |
|
|
|a Text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
| 338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
| 500 |
|
|
|a Date Completed 01.06.2016
|
| 500 |
|
|
|a Date Revised 09.04.2022
|
| 500 |
|
|
|a published: Print-Electronic
|
| 500 |
|
|
|a Citation Status MEDLINE
|
| 520 |
|
|
|a © 2015 The Authors. New Phytologist © 2015 New Phytologist Trust.
|
| 520 |
|
|
|a A minority of angiosperms have male and female flowers separated in distinct individuals (dioecy), and most dioecious plants do not have cytologically different (heteromorphic) sex chromosomes. Plants nevertheless have several advantages for the study of sex chromosome evolution, as genetic sex determination has evolved repeatedly and is often absent in close relatives. I review sex-determining regions in non-model plant species, which may help us to understand when and how (and, potentially, test hypotheses about why) recombination suppression evolves within young sex chromosomes. I emphasize high-throughput sequencing approaches that are increasingly being applied to plants to test for non-recombining regions. These data are particularly illuminating when combined with sequence data that allow phylogenetic analyses, and estimates of when these regions evolved. Together with comparative genetic mapping, this has revealed that sex-determining loci and sex-linked regions evolved independently in many plant lineages, sometimes in closely related dioecious species, and often within the past few million years. In reviewing recent progress, I suggest areas for future work, such as the use of phylogenies to allow the informed choice of outgroup species suitable for inferring the directions of changes, including testing whether Y chromosome-like regions are undergoing genetic degeneration, a predicted consequence of losing recombination
|
| 650 |
|
4 |
|a Journal Article
|
| 650 |
|
4 |
|a Review
|
| 650 |
|
4 |
|a genetic degeneration
|
| 650 |
|
4 |
|a partial sex linkage
|
| 650 |
|
4 |
|a recombination suppression
|
| 650 |
|
4 |
|a sex chromosomes
|
| 650 |
|
4 |
|a sex determination
|
| 773 |
0 |
8 |
|i Enthalten in
|t The New phytologist
|d 1979
|g 208(2015), 1 vom: 08. Okt., Seite 52-65
|w (DE-627)NLM09818248X
|x 1469-8137
|7 nnas
|
| 773 |
1 |
8 |
|g volume:208
|g year:2015
|g number:1
|g day:08
|g month:10
|g pages:52-65
|
| 856 |
4 |
0 |
|u http://dx.doi.org/10.1111/nph.13497
|3 Volltext
|
| 912 |
|
|
|a GBV_USEFLAG_A
|
| 912 |
|
|
|a SYSFLAG_A
|
| 912 |
|
|
|a GBV_NLM
|
| 912 |
|
|
|a GBV_ILN_350
|
| 951 |
|
|
|a AR
|
| 952 |
|
|
|d 208
|j 2015
|e 1
|b 08
|c 10
|h 52-65
|